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Article

Diverse and novel RHD variants in Australian blood donors with a weak D phenotype: implication for transfusion management. McGowan EC, Lopez GH, Knauth CM, Liew YW, Condon JA, Ramadi L, Parsons K, Turner EM, Flower RL, Hyland CA. Vox Sang, 2017. [Citation]

Annotations by Allele

  • apparently standard RHD with unexpected serology: RH1
  • apparently standard RHD with unexpected serology: otherHaplotype
  • apparently standard RHD with unexpected serology: otherHaplotype
  • RHD*1154C (weak D type 2): otherHaplotype
  • RHD*1154C (weak D type 2): Prevalence
  • RHD*1154C (weak D type 2): RH1
  • RHD*1154C (weak D type 2): otherHaplotype
  • RHD*1154C (weak D type 2): otherHaplotype
  • RHD*1177C (weak D type 10): RH1
  • RHD*1177C (weak D type 10): otherHaplotype
  • RHD*1177C (weak D type 10): Prevalence
  • RHD*329C (DVII): otherHaplotype
  • RHD*329C (DVII): Prevalence
  • RHD*329C (DVII): RH1
  • RHD*340T (weak D type 17): RH1
  • RHD*340T (weak D type 17): otherHaplotype
  • RHD*340T (weak D type 17): Prevalence
  • RHD*446A (weak D type 5): RH1
  • RHD*446A (weak D type 5): otherHaplotype
  • RHD*446A (weak D type 5): Prevalence
  • RHD*48C,602G,667G,819A (weak D type 4.1, DAR4): RH1
  • RHD*48C,602G,667G,819A (weak D type 4.1, DAR4): otherHaplotype
  • RHD*48C,602G,667G,819A (weak D type 4.1, DAR4): Prevalence
  • RHD*520A (weak D type 33): RH1
  • RHD*520A (weak D type 33): otherHaplotype
  • RHD*520A (weak D type 33): Prevalence
  • RHD*52G,809G (weak D type 1.1): RH1
  • RHD*52G,809G (weak D type 1.1): otherHaplotype
  • RHD*52G,809G (weak D type 1.1): Prevalence
  • RHD*602G,667G,819A (weak D type 4.0, DAR3.01): Prevalence
  • RHD*602G,667G,819A (weak D type 4.0, DAR3.01): RH1
  • RHD*602G,667G,819A (weak D type 4.0, DAR3.01): otherHaplotype
  • RHD*676C (DCS2, RHD*16.02): Prevalence
  • RHD*676C (DCS2, RHD*16.02): RH1
  • RHD*676C (DCS2, RHD*16.02): otherHaplotype
  • RHD*680C (DBA, RHD*56): RH1
  • RHD*680C (DBA, RHD*56): otherHaplotype
  • RHD*680C (DBA, RHD*56): Prevalence
  • RHD*697A (DV type 5, DHK): RH1
  • RHD*697A (DV type 5, DHK): otherHaplotype
  • RHD*697A (DV type 5, DHK): Prevalence
  • RHD*809G (weak D type 1): otherHaplotype
  • RHD*809G (weak D type 1): Prevalence
  • RHD*809G (weak D type 1): RH1
  • RHD*809G (weak D type 1): otherHaplotype
  • RHD*809G (weak D type 1): otherHaplotype
  • RHD*845A (weak partial D type 15): Prevalence
  • RHD*845A (weak partial D type 15): RH1
  • RHD*845A (weak partial D type 15): otherHaplotype
  • RHD*885T (weak partial D type 11): RH1
  • RHD*885T (weak partial D type 11): otherHaplotype
  • RHD*885T (weak partial D type 11): Prevalence
  • RHD*8G (weak D type 3): RH1
  • RHD*8G (weak D type 3): otherHaplotype
  • RHD*8G (weak D type 3): otherHaplotype
  • RHD*8G (weak D type 3): Prevalence
  • RHD*939+3C (IVS6+3C): RH1
  • RHD*939+3C (IVS6+3C): otherHaplotype
  • RHD*939+3C (IVS6+3C): Prevalence
  • RHD*993G (weak D type 90): otherHaplotype
  • RHD*993G (weak D type 90): Prevalence
  • RHD*993G (weak D type 90): RH1
  • RHD*D-CE(4-6)-D (DVI type 2): RH1
  • RHD*D-CE(4-6)-D (DVI type 2): otherHaplotype
  • RHD*D-CE(4-6)-D (DVI type 2): Prevalence