Canonical Allele Identifier: CA136832921

Gene: HLA-B

Linked Data

• dbSNP Id: rs74353323
• gnomAD v3: 6-31355503-T-C
• gnomAD v4: 6-31355503-T-C
• MyVariant Identifiers: chr6:g.31323280T>C (hg19) ; chr6:g.31355503T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355503T>C , CM000668.2:g.31355503T>C	GRCh38
NC_000006.11:g.31323280T>C , CM000668.1:g.31323280T>C	GRCh37
NC_000006.10:g.31431259T>C	NCBI36
NG_023187.1:g.6710A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2756A>G
ENST00000481849.6:n.2182A>G
ENST00000497377.6:n.2182A>G
ENST00000640094.2:c.709A>G	ENSP00000491275.2:p.Ile237Val
ENST00000696558.1:c.778A>G	ENSP00000512716.1:n.778A>G
ENST00000696559.1:c.709A>G	ENSP00000512717.1:p.Ile237Val
ENST00000696560.1:c.709A>G	ENSP00000512718.1:p.Ile237Val
ENST00000696561.1:c.709A>G	ENSP00000512719.1:p.Ile237Val
ENST00000696562.1:c.709A>G	ENSP00000512720.1:p.Ile237Val
ENST00000412585.7:c.709A>G MANE Select	ENSP00000399168.2:p.Ile237Val
ENST00000412585.6:c.709A>G	ENSP00000399168.2:p.Ile237Val
ENST00000463574.1:n.300A>G
ENST00000498007.1:n.975A>G
NM_005514.6:c.709A>G	NP_005505.2:p.Ile237Val
XM_011514556.1:c.742A>G	XP_011512858.1:p.Ile248Val
XM_011514557.1:c.709A>G	XP_011512859.1:p.Ile237Val
XR_926175.1:n.1148A>G
NM_005514.7:c.709A>G	NP_005505.2:p.Ile237Val
NM_005514.8:c.709A>G MANE Select	NP_005505.2:p.Ile237Val