Canonical Allele Identifier: CA2677958295
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357543_31357544insAT , CM000668.2:g.31357543_31357544insAT GRCh38
NC_000006.11:g.31325320_31325321insAT , CM000668.1:g.31325320_31325321insAT GRCh37
NC_000006.10:g.31433299_31433300insAT NCBI36
NG_023187.1:g.4669_4670insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1338+70_1338+71insAT
ENST00000481849.6:n.1338+70_1338+71insAT
ENST00000497377.6:n.1338+70_1338+71insAT
ENST00000696559.1:c.-136+70_-136+71insAT ENSP00000512717.1:n.-136+70_-136+71insAT
ENST00000696560.1:c.-136+70_-136+71insAT ENSP00000512718.1:n.-136+70_-136+71insAT
ENST00000696561.1:c.-136+70_-136+71insAT ENSP00000512719.1:n.-136+70_-136+71insAT
ENST00000696562.1:c.-135-251_-135-250insAT ENSP00000512720.1:n.-135-251_-135-250insAT
ENST00000603274.1:n.897_898insAT
XR_926692.1:n.164+70_164+71insAT