RHD*667G,697C,733C,744T
(ISBT table: not listed)
				This entry is an RHD allele.
						RHD(F223V,E233Q,V245L), RHD(F223V,E233Q,V245L,S248S), RHD*667G,697C,733C,744T, RHD*667T>G,697G>C,733G>C,744C>T, 
					
	
				Molecular data
Phenotype
Main D phenotype: weak D (last update: Aug. 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: unknown (last update: Dec. 9, 2020)| ce | Ce | cE | CE | |
|---|---|---|---|---|
| ce | 0 | 0 | 0 | 0 | 
| Ce | 0 | 0 | 0 | |
| cE | 0 | 0 | ||
| CE | 0 | 
Reports by CcEe phenotype
Reports by allele association
Alloimmunization
Antibodies in carriers
Antibody specificity: D (RH1)
Summary: no published cases (last update: Aug. 9, 2020)Detailed information
Antibodies in D negative recipients
Alloimmunization in recipients: expected to be possible, see phenotype data
Reports
Summary: (last update: Aug. 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
- Trina Horn et al. Four Novel RHD Alleles Identified Through Investigation of Discrepant or Weak D Status Transfusion, 2019. — Abstract — [RHeference]
 - Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
 
Last update: Aug. 9, 2020