Canonical Allele Identifier: CA363308484

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31355119-T-C
• gnomAD v4: 6-31355119-T-C
• MyVariant Identifiers: chr6:g.31322896T>C (hg19) ; chr6:g.31355119T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355119T>C , CM000668.2:g.31355119T>C	GRCh38
NC_000006.11:g.31322896T>C , CM000668.1:g.31322896T>C	GRCh37
NC_000006.10:g.31430875T>C	NCBI36
NG_023187.1:g.7094A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3047A>G
ENST00000481849.6:n.2566A>G
ENST00000497377.6:n.2473A>G
ENST00000640094.2:c.895+198A>G	ENSP00000491275.2:n.895+198A>G
ENST00000696558.1:c.1069A>G	ENSP00000512716.1:n.1069A>G
ENST00000696559.1:c.1000A>G	ENSP00000512717.1:p.Arg334Gly
ENST00000696560.1:c.1000A>G	ENSP00000512718.1:p.Arg334Gly
ENST00000696561.1:c.1000A>G	ENSP00000512719.1:p.Arg334Gly
ENST00000696562.1:c.1000A>G	ENSP00000512720.1:p.Arg334Gly
ENST00000412585.7:c.1000A>G MANE Select	ENSP00000399168.2:p.Arg334Gly
ENST00000640094.1:c.88+198A>G	ENSP00000491275.1:n.88+198A>G
ENST00000412585.6:c.1000A>G	ENSP00000399168.2:p.Arg334Gly
NM_005514.6:c.1000A>G	NP_005505.2:p.Arg334Gly
XM_011514556.1:c.1033A>G	XP_011512858.1:p.Arg345Gly
XM_011514557.1:c.895+198A>G	XP_011512859.1:n.895+198A>G
XR_926175.1:n.1439A>G
NM_005514.7:c.1000A>G	NP_005505.2:p.Arg334Gly
NM_005514.8:c.1000A>G MANE Select	NP_005505.2:p.Arg334Gly