Canonical Allele Identifier: CA2677958284
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357532_31357533insA , CM000668.2:g.31357532_31357533insA GRCh38
NC_000006.11:g.31325309_31325310insA , CM000668.1:g.31325309_31325310insA GRCh37
NC_000006.10:g.31433288_31433289insA NCBI36
NG_023187.1:g.4680_4681insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1338+81_1338+82insT
ENST00000481849.6:n.1338+81_1338+82insT
ENST00000497377.6:n.1338+81_1338+82insT
ENST00000696559.1:c.-136+81_-136+82insT ENSP00000512717.1:n.-136+81_-136+82insT
ENST00000696560.1:c.-136+81_-136+82insT ENSP00000512718.1:n.-136+81_-136+82insT
ENST00000696561.1:c.-136+81_-136+82insT ENSP00000512719.1:n.-136+81_-136+82insT
ENST00000696562.1:c.-135-240_-135-239insT ENSP00000512720.1:n.-135-240_-135-239insT
ENST00000603274.1:n.886_887insA
XR_926692.1:n.164+81_164+82insT