Canonical Allele Identifier: CA449601255

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31355144-A-C
• gnomAD v4: 6-31355144-A-C
• MyVariant Identifiers: chr6:g.31322921A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355144A>C , CM000668.2:g.31355144A>C	GRCh38
NC_000006.11:g.31322921A>C , CM000668.1:g.31322921A>C	GRCh37
NC_000006.10:g.31430900A>C	NCBI36
NG_023187.1:g.7069T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3022T>G
ENST00000481849.6:n.2541T>G
ENST00000497377.6:n.2448T>G
ENST00000640094.2:c.895+173T>G	ENSP00000491275.2:n.895+173T>G
ENST00000696558.1:c.1044T>G	ENSP00000512716.1:n.1044T>G
ENST00000696559.1:c.975T>G	ENSP00000512717.1:p.Ala325=
ENST00000696560.1:c.975T>G	ENSP00000512718.1:p.Ala325=
ENST00000696561.1:c.975T>G	ENSP00000512719.1:p.Ala325=
ENST00000696562.1:c.975T>G	ENSP00000512720.1:p.Ala325=
ENST00000412585.7:c.975T>G MANE Select	ENSP00000399168.2:p.Ala325=
ENST00000640094.1:c.88+173T>G	ENSP00000491275.1:n.88+173T>G
ENST00000412585.6:c.975T>G	ENSP00000399168.2:p.Ala325=
ENST00000463574.1:n.566T>G
NM_005514.6:c.975T>G	NP_005505.2:p.Ala325=
XM_011514556.1:c.1008T>G	XP_011512858.1:p.Ala336=
XM_011514557.1:c.895+173T>G	XP_011512859.1:n.895+173T>G
XR_926175.1:n.1414T>G
NM_005514.7:c.975T>G	NP_005505.2:p.Ala325=
NM_005514.8:c.975T>G MANE Select	NP_005505.2:p.Ala325=