Canonical Allele Identifier: CA449599647

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31354658-T-C
• gnomAD v4: 6-31354658-T-C
• MyVariant Identifiers: chr6:g.31322435T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354658T>C , CM000668.2:g.31354658T>C	GRCh38
NC_000006.11:g.31322435T>C , CM000668.1:g.31322435T>C	GRCh37
NC_000006.10:g.31430414T>C	NCBI36
NG_023187.1:g.7555A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3067A>G
ENST00000481849.6:n.3027A>G
ENST00000497377.6:n.2934A>G
ENST00000640094.2:c.903A>G	ENSP00000491275.2:p.Lys301=
ENST00000696558.1:c.1089A>G	ENSP00000512716.1:n.1089A>G
ENST00000696559.1:c.1020A>G	ENSP00000512717.1:p.Lys340=
ENST00000696560.1:c.1020A>G	ENSP00000512718.1:p.Lys340=
ENST00000696561.1:c.1020A>G	ENSP00000512719.1:p.Lys340=
ENST00000696562.1:c.1020A>G	ENSP00000512720.1:p.Lys340=
ENST00000412585.7:c.1020A>G MANE Select	ENSP00000399168.2:p.Lys340=
ENST00000640094.1:c.96A>G	ENSP00000491275.1:p.Lys32=
ENST00000412585.6:c.1020A>G	ENSP00000399168.2:p.Lys340=
ENST00000481849.5:n.149A>G
ENST00000497377.5:n.419A>G
NM_005514.6:c.1020A>G	NP_005505.2:p.Lys340=
XM_011514556.1:c.1053A>G	XP_011512858.1:p.Lys351=
XM_011514557.1:c.903A>G	XP_011512859.1:p.Lys301=
XR_926175.1:n.1459A>G
NM_005514.7:c.1020A>G	NP_005505.2:p.Lys340=
NM_005514.8:c.1020A>G MANE Select	NP_005505.2:p.Lys340=