RHD*739C
(ISBT table: not listed)
This entry is an RHD allele.
RHD(V247L), RHD*739C, RHD*739G>C,
Molecular data
Phenotype
Main D phenotype: weak D (last update: Dec. 9, 2020)Reports by D phenotype
Other RH phenotypes: RH:
Serology with monoclonal anti-D
Antigen Density (Ag/RBC)
More phenotype data
Rhesus Similarity Index
Haplotype
Main CcEe phenotype association: ce (last update: Dec. 9, 2020)Alloimmunization
Antibodies in carriers
Antibody specificity: D (RH1)
Summary: no published cases (last update: Dec. 1, 2020)Detailed information
Antibodies in D negative recipients
Alloimmunization in recipients: unknown
Reports
Summary: exceptional description(s), Chinese (last update: Dec. 9, 2020)Structure mapping
Movement | Mouse Input | Touch Input | ||
---|---|---|---|---|
Rotation | Primary Mouse Button | Single touch | ||
Translation | Middle Mouse Button or Ctrl+Primary | Triple touch | ||
Zoom | Scroll Wheel or Second Mouse Button or Shift+Primary | Pinch (double touch) | ||
Slab | Ctrl+Second | Not Available |
References
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
- Lyu H et al. A novel RHD allele caused by c.739 G> C mutation was identified in a Chinese individual. Transfusion, 2021. [Citation] [RHeference]
Last update: Dec. 9, 2020