Canonical Allele Identifier: CA449599663

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31354661-T-C
• gnomAD v4: 6-31354661-T-C
• MyVariant Identifiers: chr6:g.31322438T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354661T>C , CM000668.2:g.31354661T>C	GRCh38
NC_000006.11:g.31322438T>C , CM000668.1:g.31322438T>C	GRCh37
NC_000006.10:g.31430417T>C	NCBI36
NG_023187.1:g.7552A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3064A>G
ENST00000481849.6:n.3024A>G
ENST00000497377.6:n.2931A>G
ENST00000640094.2:c.900A>G	ENSP00000491275.2:p.Gly300=
ENST00000696558.1:c.1086A>G	ENSP00000512716.1:n.1086A>G
ENST00000696559.1:c.1017A>G	ENSP00000512717.1:p.Gly339=
ENST00000696560.1:c.1017A>G	ENSP00000512718.1:p.Gly339=
ENST00000696561.1:c.1017A>G	ENSP00000512719.1:p.Gly339=
ENST00000696562.1:c.1017A>G	ENSP00000512720.1:p.Gly339=
ENST00000412585.7:c.1017A>G MANE Select	ENSP00000399168.2:p.Gly339=
ENST00000640094.1:c.93A>G	ENSP00000491275.1:p.Gly31=
ENST00000412585.6:c.1017A>G	ENSP00000399168.2:p.Gly339=
ENST00000481849.5:n.146A>G
ENST00000497377.5:n.416A>G
NM_005514.6:c.1017A>G	NP_005505.2:p.Gly339=
XM_011514556.1:c.1050A>G	XP_011512858.1:p.Gly350=
XM_011514557.1:c.900A>G	XP_011512859.1:p.Gly300=
XR_926175.1:n.1456A>G
NM_005514.7:c.1017A>G	NP_005505.2:p.Gly339=
NM_005514.8:c.1017A>G MANE Select	NP_005505.2:p.Gly339=