Nucleotides: 662C>T;

Amino acids: P221L;

Hybrid allele encompassing at least one RHCE exon: no

Comments on the molecular basis:

Extracellular position of one or more amino acid substitutions:

• 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

• 1/129 (heterozygous with RHef00122) donors with weak D phenotype Thai

Allele or phenotype frequency