Canonical Allele Identifier: CA363308647

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31355142-A-C
• gnomAD v4: 6-31355142-A-C
• MyVariant Identifiers: chr6:g.31322919A>C (hg19) ; chr6:g.31355142A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355142A>C , CM000668.2:g.31355142A>C	GRCh38
NC_000006.11:g.31322919A>C , CM000668.1:g.31322919A>C	GRCh37
NC_000006.10:g.31430898A>C	NCBI36
NG_023187.1:g.7071T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3024T>G
ENST00000481849.6:n.2543T>G
ENST00000497377.6:n.2450T>G
ENST00000640094.2:c.895+175T>G	ENSP00000491275.2:n.895+175T>G
ENST00000696558.1:c.1046T>G	ENSP00000512716.1:n.1046T>G
ENST00000696559.1:c.977T>G	ENSP00000512717.1:p.Val326Gly
ENST00000696560.1:c.977T>G	ENSP00000512718.1:p.Val326Gly
ENST00000696561.1:c.977T>G	ENSP00000512719.1:p.Val326Gly
ENST00000696562.1:c.977T>G	ENSP00000512720.1:p.Val326Gly
ENST00000412585.7:c.977T>G MANE Select	ENSP00000399168.2:p.Val326Gly
ENST00000640094.1:c.88+175T>G	ENSP00000491275.1:n.88+175T>G
ENST00000412585.6:c.977T>G	ENSP00000399168.2:p.Val326Gly
ENST00000463574.1:n.568T>G
NM_005514.6:c.977T>G	NP_005505.2:p.Val326Gly
XM_011514556.1:c.1010T>G	XP_011512858.1:p.Val337Gly
XM_011514557.1:c.895+175T>G	XP_011512859.1:n.895+175T>G
XR_926175.1:n.1416T>G
NM_005514.7:c.977T>G	NP_005505.2:p.Val326Gly
NM_005514.8:c.977T>G MANE Select	NP_005505.2:p.Val326Gly