Article
Weak D phenotypes caused by intronic mutations in the RHD gene: four novel weak D alleles identified in the Chinese population. Ye L, He Y, Gao H, Guo Z, Zhu Z. Transfusion, 2013. [Citation]
Annotations by Allele
- RHD*486+3C (IVS3+3C): RH1
- RHD*486+3C (IVS3+3C): Serology
- RHD*486+3C (IVS3+3C): otherHaplotype
- RHD*486+3C (IVS3+3C): Prevalence
- RHD*634+5A (IVS4+5A): otherHaplotype
- RHD*634+5A (IVS4+5A): Prevalence
- RHD*634+5A (IVS4+5A): Serology (Table 1)
- RHD*634+5A (IVS4+5A): RH1
- RHD*634+5T (IVS4+5T, DEL14): RH1
- RHD*634+5T (IVS4+5T, DEL14): Serology
- RHD*634+5T (IVS4+5T, DEL14): otherHaplotype
- RHD*634+5T (IVS4+5T, DEL14): Prevalence
- RHD*940-14delTAA (IVS6-14delTAA): Serology
- RHD*940-14delTAA (IVS6-14delTAA): otherHaplotype
- RHD*940-14delTAA (IVS6-14delTAA): Prevalence
- RHD*940-14delTAA (IVS6-14delTAA): RH1