Nucleotides: 203G>C; 361T>A; 380T>C; 383A>G; 455A>C; 505A>C; 509T>G; 514A>T; 544T>A; 577G>A; 594A>T; 602C>G; 667T>G; 697G>C; 712G>A; 733G>C; 744C>T; 787G>A; 800A>T; 916G>A; 932A>G; 941G>T; 968C>A; 974G>T; 979A>G; 985GG>CA deletion-insertion; 989A>C; 992A>T; 1025T>C; 1048G>C; 1053C>T; 1057GGA>TGG deletion-insertion; 1060GC>AA deletion-insertion; 1170T>C; 1193A>T;

Amino acids: S68T; L121M; V127A; D128G; N152T; M169L; M170R; I172F; S182T; E193K; K198N; T201R; F223V; E233Q; V238M; V245L; S248S; G263R; K267M; V306I; Y311C; G314V; P323H; S325I; I327V; G329H; Y330S; N331I; I342T; D350H; T351T; G353W; A354N; L390L; E398V;

Hybrid allele encompassing at least one RHCE exon: RHD(S68T)-RHCE(3-9)-RHD

Comments on the molecular basis:

• see also "Additional comments" section on the RhesusBase http://www.rhesusbase.info/RHDRHD(S68T)-RHCe(3-9)-RHD.htm
• may be a typo in the Genbank description? No publications found referring to this molecular description. See RHef00448 RHD-RHCe(2-9)-RHD

Extracellular position of one or more amino acid substitutions:

• hybrid RHD-RHCE, several residues are predicted to be extracellular

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: NA

Detailed reports

Allele or phenotype frequency