Canonical Allele Identifier: CA136832654
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs151341388

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355319del , CM000668.2:g.31355319del GRCh38
NC_000006.11:g.31323096del , CM000668.1:g.31323096del GRCh37
NC_000006.10:g.31431075del NCBI36
NG_023187.1:g.6897del

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2942+1del
ENST00000481849.6:n.2369del
ENST00000497377.6:n.2368+1del
ENST00000640094.2:c.895+1del
ENST00000696558.1:c.964+1del
ENST00000696559.1:c.895+1del
ENST00000696560.1:c.895+1del
ENST00000696561.1:c.895+1del
ENST00000696562.1:c.895+1del
ENST00000412585.7:c.895+1del
ENST00000640094.1:c.88+1del
ENST00000412585.6:c.895+1del
ENST00000463574.1:n.486+1del
NM_005514.6:c.895+1del
XM_011514556.1:c.928+1del
XM_011514557.1:c.895+1del
XR_926175.1:n.1334+1del
NM_005514.7:c.895+1del
NM_005514.8:c.895+1del