Canonical Allele Identifier: CA363311030

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31355496-A-C
• gnomAD v4: 6-31355496-A-C
• MyVariant Identifiers: chr6:g.31323273A>C (hg19) ; chr6:g.31355496A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355496A>C , CM000668.2:g.31355496A>C	GRCh38
NC_000006.11:g.31323273A>C , CM000668.1:g.31323273A>C	GRCh37
NC_000006.10:g.31431252A>C	NCBI36
NG_023187.1:g.6717T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2763T>G
ENST00000481849.6:n.2189T>G
ENST00000497377.6:n.2189T>G
ENST00000640094.2:c.716T>G	ENSP00000491275.2:p.Leu239Arg
ENST00000696558.1:c.785T>G	ENSP00000512716.1:n.785T>G
ENST00000696559.1:c.716T>G	ENSP00000512717.1:p.Leu239Arg
ENST00000696560.1:c.716T>G	ENSP00000512718.1:p.Leu239Arg
ENST00000696561.1:c.716T>G	ENSP00000512719.1:p.Leu239Arg
ENST00000696562.1:c.716T>G	ENSP00000512720.1:p.Leu239Arg
ENST00000412585.7:c.716T>G MANE Select	ENSP00000399168.2:p.Leu239Arg
ENST00000412585.6:c.716T>G	ENSP00000399168.2:p.Leu239Arg
ENST00000463574.1:n.307T>G
ENST00000498007.1:n.982T>G
NM_005514.6:c.716T>G	NP_005505.2:p.Leu239Arg
XM_011514556.1:c.749T>G	XP_011512858.1:p.Leu250Arg
XM_011514557.1:c.716T>G	XP_011512859.1:p.Leu239Arg
XR_926175.1:n.1155T>G
NM_005514.7:c.716T>G	NP_005505.2:p.Leu239Arg
NM_005514.8:c.716T>G MANE Select	NP_005505.2:p.Leu239Arg