Canonical Allele Identifier: CA363307887

Gene: HLA-B

Linked Data

• MyVariant Identifiers: chr6:g.31322276A>C (hg19) ; chr6:g.31354499A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354499A>C , CM000668.2:g.31354499A>C	GRCh38
NC_000006.11:g.31322276A>C , CM000668.1:g.31322276A>C	GRCh37
NC_000006.10:g.31430255A>C	NCBI36
NG_023187.1:g.7714T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3120T>G
ENST00000481849.6:n.3080T>G
ENST00000497377.6:n.2987T>G
ENST00000640094.2:c.956T>G	ENSP00000491275.2:p.Val319Gly
ENST00000696558.1:c.1142T>G	ENSP00000512716.1:n.1142T>G
ENST00000696559.1:c.1073T>G	ENSP00000512717.1:p.Val358Gly
ENST00000696560.1:c.1073T>G	ENSP00000512718.1:p.Val358Gly
ENST00000696561.1:c.1073T>G	ENSP00000512719.1:p.Val358Gly
ENST00000696562.1:c.1073T>G	ENSP00000512720.1:p.Val358Gly
ENST00000412585.7:c.1073T>G MANE Select	ENSP00000399168.2:p.Val358Gly
ENST00000412585.6:c.1073T>G	ENSP00000399168.2:p.Val358Gly
ENST00000481849.5:n.308T>G
ENST00000497377.5:n.472T>G
NM_005514.6:c.1073T>G	NP_005505.2:p.Val358Gly
XM_011514556.1:c.1106T>G	XP_011512858.1:p.Val369Gly
XM_011514557.1:c.956T>G	XP_011512859.1:p.Val319Gly
XR_926175.1:n.1512T>G
NM_005514.7:c.1073T>G	NP_005505.2:p.Val358Gly
NM_005514.8:c.1073T>G MANE Select	NP_005505.2:p.Val358Gly