RHD*DIII-CE(9)-D(604A)
(ISBT table: not listed)
				This entry is an hybrid RHD allele.
						RHD*186T,410T,455C,602G,604A,733C,1170C,1193T, RHD*DIII-CE(9)-D, RHD*DIII-CE(9)-D(604A), RHD*DIII-CE(9)-D(604G>A), 
					
	
				Molecular data
						Nucleotides:
						186G>T; 410C>T; 455A>C; 602C>G; 604G>A; 733G>C; 1170T>C; 1193A>T; 
					
Amino acids: L62F; A137V; N152T; T201R; A202T; V245L; L390L; E398V;
						Hybrid allele encompassing at least one  RHCE  exon:
						RHD(DIII)-RHCE(9)-RHD
					
						Comments on the molecular basis:
						
						Extracellular position of one or more amino acid substitutions: 
						
						Splicing:
						
						Unconventional prediction methods:
						
Phenotype
Main D phenotype: D positive (last update: March 7, 2020)Reports by D phenotype
Other RH phenotypes: RH:-33, -50,
Serology with monoclonal anti-D
Antigen Density (Ag/RBC)
More phenotype data
Rhesus Similarity Index
Haplotype
Main CcEe phenotype association: ce (last update: March 7, 2020)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: yes, see detailed reports and phenotype data
Reports
Summary: exceptional description(s), in the Australian population; expected to be an allele of African descent (last update: March 7, 2020)Structure mapping
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References
- J Morrison et al. Severe case of haemolytic disease of fetus and newborn occurring in baby who has inherited a novel RHD allele associated with a “partial” RhD positive phenotype Vox Sanguinis, 2019. — Abstract — [RHeference]
 - Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
 
Last update: March 7, 2020