Canonical Allele Identifier: CA1619114826
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357458_31357459delinsCA , CM000668.2:g.31357458_31357459delinsCA GRCh38
NC_000006.11:g.31325235_31325236delinsCA , CM000668.1:g.31325235_31325236delinsCA GRCh37
NC_000006.10:g.31433214_31433215delinsCA NCBI36
NG_023187.1:g.4754_4755delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1338+155_1338+156delinsTG
ENST00000481849.6:n.1338+155_1338+156delinsTG
ENST00000497377.6:n.1338+155_1338+156delinsTG
ENST00000696559.1:c.-136+155_-136+156delinsTG ENSP00000512717.1:n.-136+155_-136+156delinsTG
ENST00000696560.1:c.-136+155_-136+156delinsTG ENSP00000512718.1:n.-136+155_-136+156delinsTG
ENST00000696561.1:c.-136+155_-136+156delinsTG ENSP00000512719.1:n.-136+155_-136+156delinsTG
ENST00000696562.1:c.-135-166_-135-165delinsTG ENSP00000512720.1:n.-135-166_-135-165delinsTG
ENST00000603274.1:n.812_813delinsCA
XR_926692.1:n.164+155_164+156delinsTG