Canonical Allele Identifier: CA363308864

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31355166-A-G
• gnomAD v4: 6-31355166-A-G
• MyVariant Identifiers: chr6:g.31322943A>G (hg19) ; chr6:g.31355166A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3000T>C
ENST00000481849.6:n.2519T>C
ENST00000497377.6:n.2426T>C
ENST00000640094.2:c.895+151T>C	ENSP00000491275.2:n.895+151T>C
ENST00000696558.1:c.1022T>C	ENSP00000512716.1:n.1022T>C
ENST00000696559.1:c.953T>C	ENSP00000512717.1:p.Leu318Pro
ENST00000696560.1:c.953T>C	ENSP00000512718.1:p.Leu318Pro
ENST00000696561.1:c.953T>C	ENSP00000512719.1:p.Leu318Pro
ENST00000696562.1:c.953T>C	ENSP00000512720.1:p.Leu318Pro
ENST00000412585.7:c.953T>C MANE Select	ENSP00000399168.2:p.Leu318Pro
ENST00000640094.1:c.88+151T>C	ENSP00000491275.1:n.88+151T>C
ENST00000412585.6:c.953T>C	ENSP00000399168.2:p.Leu318Pro
ENST00000463574.1:n.544T>C
NM_005514.6:c.953T>C	NP_005505.2:p.Leu318Pro
XM_011514556.1:c.986T>C	XP_011512858.1:p.Leu329Pro
XM_011514557.1:c.895+151T>C	XP_011512859.1:n.895+151T>C
XR_926175.1:n.1392T>C
NM_005514.7:c.953T>C	NP_005505.2:p.Leu318Pro
NM_005514.8:c.953T>C MANE Select	NP_005505.2:p.Leu318Pro