Article
In-frame triplet deletions in RHD alter the D antigen phenotype. Flegel WA, Eicher NI, Doescher A, Hustinx H, Gowland P, Mansouri Taleghani B, Petershofen EK, Bauerfeind U, Ernst M, von Zabern I, Schrezenmeier H, Wagner FF. Transfusion, 2006. [Citation]
Annotations by Allele
- RHD*684_686delGAG (DVL1, RHD*31): RH1 (initially typed as D negative)
- RHD*684_686delGAG (DVL1, RHD*31): Serology
- RHD*684_686delGAG (DVL1, RHD*31): Density
- RHD*684_686delGAG (DVL1, RHD*31): otherHaplotype (considered most likely haplotype)
- RHD*684_686delGAG (DVL1, RHD*31): Prevalence
- RHD*684_686delGAG (DVL1, RHD*31): RH1
- RHD*705_707delGAA (DVL2, RHD*32): Density
- RHD*705_707delGAA (DVL2, RHD*32): otherHaplotype (considered most likely haplotype)
- RHD*705_707delGAA (DVL2, RHD*32): Prevalence
- RHD*705_707delGAA (DVL2, RHD*32): RH1
- RHD*705_707delGAA (DVL2, RHD*32): RH1 (initially typed as D negative)
- RHD*705_707delGAA (DVL2, RHD*32): Serology
- RHD*D-CE(5)-D (DV type 2, Hus): Serology