RHD*654C
(ISBT table: not listed)
				This entry is not counted as an allele.
						RHD(M218I), RHD*654C, RHD*654G>C, 
					
	
				Molecular data
						Nucleotides:
						654G>C; 
					
Amino acids: M218I;
						Hybrid allele encompassing at least one  RHCE  exon:
						no
					
						Comments on the molecular basis:
						
- see also "Descriptions" section on the http://www.rhesusbase.info/RHDstandardRHD.htm
 - considered to be a sequencing error
 - results are in favour of the sequencing error
 - confirms sequencing error
 - confirms sequencing error
 
						Extracellular position of one or more amino acid substitutions: 
						
						Splicing:
						
						Unconventional prediction methods:
						
Phenotype
Main D phenotype: D positive (last update: Dec. 20, 2019)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: NA (last update: Aug. 15, 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: not relevant, see types or alleles (last update: Aug. 25, 2020)Detailed information
Antibodies in D negative recipients
Alloimmunization in recipients: NA
Reports
Summary: NA, NA (last update: Aug. 25, 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
- National Center for Biotechnology Information et al. Data from Genbank submission Online ressource, 1982. — Online ressource — [RHeference]
 - Le van Kim C et al. Molecular cloning and primary structure of the human blood group RhD polypeptide. Proc Natl Acad Sci U S A, 1992. [Citation] [RHeference]
 - Cartron JP et al. Tentative model for the mapping of D epitopes on the RhD polypeptide. Transfus Clin Biol, 1996. [Citation] [RHeference]
 - Okuda H et al. The RHD gene is highly detectable in RhD-negative Japanese donors. J Clin Invest, 1997. [Citation] [RHeference]
 - Wagner FF et al. Molecular basis of weak D phenotypes. Blood, 1999. [Citation] [RHeference]
 - Legler TJ et al. RHD sequencing: a new tool for decision making on transfusion therapy and provision of Rh prophylaxis. Transfus Med, 2001. [Citation] [RHeference]
 - Wagner FF and Flegel WA et al. The Human RhesusBase Online ressource, 2011. — Online ressource — [RHeference]
 
Last update: April 21, 2020