RHD*396_397insGG
(ISBT table: not listed)
This entry is an RHD allele.
RHD*396_397insGG, RHD*396insGG, RHD*c.393–394 dupGG,
Molecular data
Phenotype
Main D phenotype: D negative (DEL not excluded) (last update: Jan. 6, 2021)Reports by D phenotype
- D negative
- Very weak D phenotype in a sample heterozygous with RHef00017
Other RH phenotypes: RH:-2, -3,
Serology with monoclonal anti-D
Antigen Density (Ag/RBC)
More phenotype data
Rhesus Similarity Index
Haplotype
Main CcEe phenotype association: ce (last update: Jan. 6, 2021)Alloimmunization
Antibodies in carriers
Antibody specificity: D (RH1)
Summary: D negative, at risk for anti-D (last update: Jan. 6, 2021)Detailed information
Antibodies in D negative recipients
Alloimmunization in recipients: not expected, see phenotype data
Reports
Summary: exceptional description(s), in the Finnish population and possibly in the German population (last update: Jan. 6, 2021)Structure mapping
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References
- Karnot A. et al. Weak RhD phenotype caused by compound heterozygosity for DAU-2 and a new RHD*c393-394 dupGG-mutation Transfus Med Hemother, 2016. — Abstract — [RHeference]
- Tammi SM et al. Next-generation sequencing of 35 RHD variants in 16 253 serologically D- pregnant women in the Finnish population. Blood Adv, 2020. [Citation] [RHeference]
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
Last update: Jan. 6, 2021