Nucleotides: 541C>T;

Amino acids: L181L;

Hybrid allele encompassing at least one RHCE exon: no

Comments on the molecular basis:

• undetailed molecular analysis, allele deduced from name provided

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:

Reports by D phenotype

Other RH phenotypes: RH:

Serology with monoclonal anti-D

Antigen Density (Ag/RBC)

More phenotype data

Reports by CcEe phenotype

Reports by allele association

Antibodies in D negative recipients

Alloimmunization in recipients: unknown

Detailed reports

• 1 or more among 829 samples African American (in the USA population)
• 1 heterozygote among 278 samples selected for the development of nonspecific quantitative next-generation sequencing. (non-random samples, may have been reported in other studies)

Allele or phenotype frequency