Canonical Allele Identifier: CA363308635

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31355139-A-G
• gnomAD v4: 6-31355139-A-G
• MyVariant Identifiers: chr6:g.31322916A>G (hg19) ; chr6:g.31355139A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355139A>G , CM000668.2:g.31355139A>G	GRCh38
NC_000006.11:g.31322916A>G , CM000668.1:g.31322916A>G	GRCh37
NC_000006.10:g.31430895A>G	NCBI36
NG_023187.1:g.7074T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3027T>C
ENST00000481849.6:n.2546T>C
ENST00000497377.6:n.2453T>C
ENST00000640094.2:c.895+178T>C	ENSP00000491275.2:n.895+178T>C
ENST00000696558.1:c.1049T>C	ENSP00000512716.1:n.1049T>C
ENST00000696559.1:c.980T>C	ENSP00000512717.1:p.Val327Ala
ENST00000696560.1:c.980T>C	ENSP00000512718.1:p.Val327Ala
ENST00000696561.1:c.980T>C	ENSP00000512719.1:p.Val327Ala
ENST00000696562.1:c.980T>C	ENSP00000512720.1:p.Val327Ala
ENST00000412585.7:c.980T>C MANE Select	ENSP00000399168.2:p.Val327Ala
ENST00000640094.1:c.88+178T>C	ENSP00000491275.1:n.88+178T>C
ENST00000412585.6:c.980T>C	ENSP00000399168.2:p.Val327Ala
ENST00000463574.1:n.571T>C
NM_005514.6:c.980T>C	NP_005505.2:p.Val327Ala
XM_011514556.1:c.1013T>C	XP_011512858.1:p.Val338Ala
XM_011514557.1:c.895+178T>C	XP_011512859.1:n.895+178T>C
XR_926175.1:n.1419T>C
NM_005514.7:c.980T>C	NP_005505.2:p.Val327Ala
NM_005514.8:c.980T>C MANE Select	NP_005505.2:p.Val327Ala