Article
Molecular basis of weak D expression in the Indian population and report of a novel, predominant variant RHD allele. Fichou Y, Parchure D, Gogri H, Gopalkrishnan V, Le Maréchal C, Chen JM, Férec C, Madkaikar M, Ghosh K, Kulkarni S. Transfusion, 2018. [Citation]
Annotations by Allele
- apparently deleted RHD with unexpected serology: Prevalence
- apparently deleted RHD with unexpected serology: RH1
- apparently standard RHD with unexpected serology: AbSpecificity
- apparently standard RHD with unexpected serology: otherHaplotype
- apparently standard RHD with unexpected serology: Prevalence
- apparently standard RHD with unexpected serology: RH1
- D negative - phenotypic description: RH1
- D negative - phenotypic description: RH1 (adsorption-elution was performed)
- D negative - phenotypic description: Prevalence
- D negative - phenotypic description: Prevalence
- RHD*1154C (weak D type 2): Prevalence
- RHD*1190G (weak D type 156): RH1
- RHD*1190G (weak D type 156): Prevalence
- RHD*143G: RH1
- RHD*143G: Prevalence
- RHD*175A (weak D type 151): Prevalence
- RHD*175A (weak D type 151): RH1
- RHD*175A (weak D type 151): otherHaplotype
- RHD*187T (weak D type 152): RH1
- RHD*187T (weak D type 152): Serology
- RHD*187T (weak D type 152): Density
- RHD*187T (weak D type 152): Prevalence
- RHD*208T (weak D type 122): RH1
- RHD*208T (weak D type 122): Prevalence
- RHD*209A (weak D type 85): RH1
- RHD*209A (weak D type 85): Prevalence
- RHD*327_487-4163dup (weak D type 150): Density
- RHD*327_487-4163dup (weak D type 150): otherHaplotype
- RHD*327_487-4163dup (weak D type 150): Prevalence
- RHD*327_487-4163dup (weak D type 150): otherHaplotype
- RHD*327_487-4163dup (weak D type 150): otherHaplotype
- RHD*327_487-4163dup (weak D type 150): otherHaplotype
- RHD*327_487-4163dup (weak D type 150): RH1
- RHD*327_487-4163dup (weak D type 150): Serology
- RHD*341A (weak D type 25): RH1
- RHD*341A (weak D type 25): Prevalence
- RHD*365G (weak D type 153): Prevalence
- RHD*365G (weak D type 153): RH1
- RHD*497C (DFW, RHD*18): RH1
- RHD*497C (DFW, RHD*18): Prevalence
- RHD*602G,667G,744T,957A,1025C (weak D type 4.2.2, DAR1.02): RH1
- RHD*602G,667G,744T,957A,1025C (weak D type 4.2.2, DAR1.02): Prevalence
- RHD*648C (weak D type 154): RH1
- RHD*648C (weak D type 154): Prevalence
- RHD*667G (DFV, RHD*08.01): RH1
- RHD*667G (DFV, RHD*08.01): Prevalence
- RHD*710T (weak D type 155): RH1
- RHD*710T (weak D type 155): Serology
- RHD*710T (weak D type 155): AbSpecificity
- RHD*710T (weak D type 155): otherHaplotype
- RHD*710T (weak D type 155): Prevalence
- RHD*731T (weak D type 96): RH1
- RHD*731T (weak D type 96): Prevalence
- RHD*809G (weak D type 1): Prevalence
- RHD*8G (weak D type 3): Prevalence
- RHD*919A (weak D type 8): RH1
- RHD*919A (weak D type 8): Prevalence
- RHD*D(602G)-CE(5)-D(1025C): Prevalence
- RHD*D(602G)-CE(5)-D(1025C): RH1
- RHD*D(602G)-CE(5)-D(1025C): Serology (Table S2)
- RHD*D(602G)-CE(5)-D(1025C): otherHaplotype
- RHD*D(640T)-CE(7)-D: RH1
- RHD*D(640T)-CE(7)-D: Serology (Table S2)
- RHD*D(640T)-CE(7)-D: otherHaplotype
- RHD*D(640T)-CE(7)-D: Prevalence
- RHD*D-CE(3-4)-D (DFR5, RHD*17.05): RH1
- RHD*D-CE(3-4)-D (DFR5, RHD*17.05): Prevalence
- RHD*D-CE(3-6)-D (DVI type 3): RH1
- RHD*D-CE(3-6)-D (DVI type 3): Prevalence
- RHD*D-CE(4)-D (DFR2, RHD*17.02): RH1
- RHD*D-CE(4)-D (DFR2, RHD*17.02): Prevalence
- RHD*D-cE(4-5)-D (DVI type 1): RH1
- RHD*D-cE(4-5)-D (DVI type 1): Prevalence
- RHD*D-CE(5:697-5:744)-D: RH1
- RHD*D-CE(5:697-5:744)-D: Prevalence
- RHD*D-CE(5:697-5:744)-D: Serology (Table S2)
- RHD*D-CE(5:697-5:744)-D: otherHaplotype