Canonical Allele Identifier: CA136831178

Gene: HLA-B

Linked Data

• dbSNP Id: rs62396266
• gnomAD v2: 6-31321823-G-A
• gnomAD v3: 6-31354046-G-A
• gnomAD v4: 6-31354046-G-A
• MyVariant Identifiers: chr6:g.31321823G>A (hg19) ; chr6:g.31354046G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354046G>A , CM000668.2:g.31354046G>A	GRCh38
NC_000006.11:g.31321823G>A , CM000668.1:g.31321823G>A	GRCh37
NC_000006.10:g.31429802G>A	NCBI36
NG_023187.1:g.8167C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3391C>T
ENST00000481849.6:n.3351C>T
ENST00000497377.6:n.3258C>T
ENST00000696558.1:c.1413C>T	ENSP00000512716.1:n.1413C>T
ENST00000696559.1:c.*255C>T	ENSP00000512717.1:n.*255C>T
ENST00000696560.1:c.*255C>T	ENSP00000512718.1:n.*255C>T
ENST00000696561.1:c.*255C>T	ENSP00000512719.1:n.*255C>T
ENST00000696562.1:c.*255C>T	ENSP00000512720.1:n.*255C>T
ENST00000412585.7:c.*255C>T MANE Select	ENSP00000399168.2:n.*255C>T
ENST00000412585.6:c.*255C>T	ENSP00000399168.2:n.*255C>T
ENST00000481849.5:n.579C>T
ENST00000497377.5:n.743C>T
NM_005514.6:c.*255C>T	NP_005505.2:n.*255C>T
XM_011514556.1:c.*255C>T	XP_011512858.1:n.*255C>T
XM_011514557.1:c.*255C>T	XP_011512859.1:n.*255C>T
XR_926175.1:n.1783C>T
NM_005514.7:c.*255C>T	NP_005505.2:n.*255C>T
NM_005514.8:c.*255C>T MANE Select	NP_005505.2:n.*255C>T