RHD*1056G
(ISBT table: not listed)
				This entry is an RHD allele.
						RHD(V352V), RHD*1056C>G, RHD*1056G, 
					
	
				Molecular data
						Nucleotides:
						1056C>G; 
					
Amino acids: V352V;
						Hybrid allele encompassing at least one  RHCE  exon:
						no
					
						Comments on the molecular basis:
						
						Extracellular position of one or more amino acid substitutions: 
						
- Silent or intronic mutations: none of the mutations are predicted to affect an extracellular amino acid.
 
						Splicing:
						
						Unconventional prediction methods:
						
Phenotype
Main D phenotype: weak D (last update: Nov. 17, 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: 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: Nov. 17, 2019)Detailed information
Antibodies in D negative recipients
Alloimmunization in recipients: expected to be possible, see phenotype data
Reports
Summary: exceptional description(s), Korean (last update: Dec. 22, 2019)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
- Chun S et al. The synonymous nucleotide substitution RHD 1056C>G alters mRNA splicing associated with serologically weak D phenotype. J Clin Lab Anal, 2018. [Citation] [RHeference]
 - Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
 
Last update: May 8, 2019