Article
The R0Har RH:33 phenotype results from substitution of exon 5 of the RHCE gene by the corresponding exon of the RHD gene. Beckers EA, Faas BH, von dem Borne AE, Overbeeke MA, van Rhenen DJ, van der Schoot CE. Br J Haematol, 1996. [Citation]
Annotations by Allele
- RHCE*ce667T,697G,712G,733G,744C,787G,800A (ceHAR, ce.22): RH
- RHCE*ce667T,697G,712G,733G,744C,787G,800A (ceHAR, ce.22): otherHaplotype
- RHCE*ce667T,697G,712G,733G,744C,787G,800A (ceHAR, ce.22): rhce (1 sample? Figure 2)
- RHCE*ce667T,697G,712G,733G,744C,787G,800A (ceHAR, ce.22): Prevalence
- RHCE*ce667T,697G,712G,733G,744C,787G,800A (ceHAR, ce.22): RH1
- RHCE*ce667T,697G,712G,733G,744C,787G,800A (ceHAR, ce.22): RH
- RHCE*ce667T,697G,712G,733G,744C,787G,800A (ceHAR, ce.22): RH (weak)