Canonical Allele Identifier: CA136831361

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354181G>A , CM000668.2:g.31354181G>A	GRCh38
NC_000006.11:g.31321958G>A , CM000668.1:g.31321958G>A	GRCh37
NC_000006.10:g.31429937G>A	NCBI36
NG_023187.1:g.8032C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005514.8:c.*120C>T MANE Select	NP_005505.2:n.*120C>T
ENST00000412585.7:c.*120C>T MANE Select	ENSP00000399168.2:n.*120C>T
NM_005514.6:c.*120C>T	NP_005505.2:n.*120C>T
NM_005514.7:c.*120C>T	NP_005505.2:n.*120C>T
ENST00000412585.6:c.*120C>T	ENSP00000399168.2:n.*120C>T
ENST00000474381.2:n.3256C>T
ENST00000481849.5:n.444C>T
ENST00000481849.6:n.3216C>T
ENST00000497377.5:n.608C>T
ENST00000497377.6:n.3123C>T
ENST00000696558.1:c.1278C>T	ENSP00000512716.1:n.1278C>T
ENST00000696559.1:c.*120C>T	ENSP00000512717.1:n.*120C>T
ENST00000696560.1:c.*120C>T	ENSP00000512718.1:n.*120C>T
ENST00000696561.1:c.*120C>T	ENSP00000512719.1:n.*120C>T
ENST00000696562.1:c.*120C>T	ENSP00000512720.1:n.*120C>T
XM_011514556.1:c.*120C>T	XP_011512858.1:n.*120C>T
XM_011514557.1:c.*120C>T	XP_011512859.1:n.*120C>T
XR_926175.1:n.1648C>T