Canonical Allele Identifier: CA566689342

Gene: HLA-B

Linked Data

• dbSNP Id: rs1249036885
• gnomAD v2: 6-31322619-G-A
• gnomAD v3: 6-31354842-G-A
• gnomAD v4: 6-31354842-G-A
• MyVariant Identifiers: chr6:g.31322619G>A (hg19) ; chr6:g.31354842G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354842G>A , CM000668.2:g.31354842G>A	GRCh38
NC_000006.11:g.31322619G>A , CM000668.1:g.31322619G>A	GRCh37
NC_000006.10:g.31430598G>A	NCBI36
NG_023187.1:g.7371C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3060-177C>T
ENST00000481849.6:n.2843C>T
ENST00000497377.6:n.2750C>T
ENST00000640094.2:c.896-177C>T	ENSP00000491275.2:n.896-177C>T
ENST00000696558.1:c.1082-177C>T	ENSP00000512716.1:n.1082-177C>T
ENST00000696559.1:c.1013-177C>T	ENSP00000512717.1:n.1013-177C>T
ENST00000696560.1:c.1013-177C>T	ENSP00000512718.1:n.1013-177C>T
ENST00000696561.1:c.1013-177C>T	ENSP00000512719.1:n.1013-177C>T
ENST00000696562.1:c.1013-177C>T	ENSP00000512720.1:n.1013-177C>T
ENST00000412585.7:c.1013-177C>T MANE Select	ENSP00000399168.2:n.1013-177C>T
ENST00000640094.1:c.89-177C>T	ENSP00000491275.1:n.89-177C>T
ENST00000412585.6:c.1013-177C>T	ENSP00000399168.2:n.1013-177C>T
ENST00000497377.5:n.235C>T
NM_005514.6:c.1013-177C>T	NP_005505.2:n.1013-177C>T
XM_011514556.1:c.1046-177C>T	XP_011512858.1:n.1046-177C>T
XM_011514557.1:c.896-177C>T	XP_011512859.1:n.896-177C>T
XR_926175.1:n.1452-177C>T
NM_005514.7:c.1013-177C>T	NP_005505.2:n.1013-177C>T
NM_005514.8:c.1013-177C>T MANE Select	NP_005505.2:n.1013-177C>T