Canonical Allele Identifier: CA363308848

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355166-A-T
• MyVariant Identifiers: chr6:g.31322943A>T (hg19) ; chr6:g.31355166A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355166A>T , CM000668.2:g.31355166A>T	GRCh38
NC_000006.11:g.31322943A>T , CM000668.1:g.31322943A>T	GRCh37
NC_000006.10:g.31430922A>T	NCBI36
NG_023187.1:g.7047T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3000T>A
ENST00000481849.6:n.2519T>A
ENST00000497377.6:n.2426T>A
ENST00000640094.2:c.895+151T>A	ENSP00000491275.2:n.895+151T>A
ENST00000696558.1:c.1022T>A	ENSP00000512716.1:n.1022T>A
ENST00000696559.1:c.953T>A	ENSP00000512717.1:p.Leu318Gln
ENST00000696560.1:c.953T>A	ENSP00000512718.1:p.Leu318Gln
ENST00000696561.1:c.953T>A	ENSP00000512719.1:p.Leu318Gln
ENST00000696562.1:c.953T>A	ENSP00000512720.1:p.Leu318Gln
ENST00000412585.7:c.953T>A MANE Select	ENSP00000399168.2:p.Leu318Gln
ENST00000640094.1:c.88+151T>A	ENSP00000491275.1:n.88+151T>A
ENST00000412585.6:c.953T>A	ENSP00000399168.2:p.Leu318Gln
ENST00000463574.1:n.544T>A
NM_005514.6:c.953T>A	NP_005505.2:p.Leu318Gln
XM_011514556.1:c.986T>A	XP_011512858.1:p.Leu329Gln
XM_011514557.1:c.895+151T>A	XP_011512859.1:n.895+151T>A
XR_926175.1:n.1392T>A
NM_005514.7:c.953T>A	NP_005505.2:p.Leu318Gln
NM_005514.8:c.953T>A MANE Select	NP_005505.2:p.Leu318Gln