Canonical Allele Identifier: CA136832644
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs281864645

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355317_31355339del , CM000668.2:g.31355317_31355339del GRCh38
NC_000006.11:g.31323094_31323116del , CM000668.1:g.31323094_31323116del GRCh37
NC_000006.10:g.31431073_31431095del NCBI36
NG_023187.1:g.6875_6897del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2921_2942+1del
ENST00000481849.6:n.2347_2369del
ENST00000497377.6:n.2347_2368+1del
ENST00000640094.2:c.874_895+1del
ENST00000696558.1:c.943_964+1del
ENST00000696559.1:c.874_895+1del
ENST00000696560.1:c.874_895+1del
ENST00000696561.1:c.874_895+1del
ENST00000696562.1:c.874_895+1del
ENST00000412585.7:c.874_895+1del
ENST00000640094.1:c.67_88+1del
ENST00000412585.6:c.874_895+1del
ENST00000463574.1:n.465_486+1del
NM_005514.6:c.874_895+1del
XM_011514556.1:c.907_928+1del
XM_011514557.1:c.874_895+1del
XR_926175.1:n.1313_1334+1del
NM_005514.7:c.874_895+1del
NM_005514.8:c.874_895+1del