Canonical Allele Identifier: CA449601316

Gene: HLA-B

Linked Data

• dbSNP Id: rs1328910073
• gnomAD v2: 6-31322978-G-C
• gnomAD v4: 6-31355201-G-C
• MyVariant Identifiers: chr6:g.31322978G>C (hg19) ; chr6:g.31355201G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355201G>C , CM000668.2:g.31355201G>C	GRCh38
NC_000006.11:g.31322978G>C , CM000668.1:g.31322978G>C	GRCh37
NC_000006.10:g.31430957G>C	NCBI36
NG_023187.1:g.7012C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2965C>G
ENST00000481849.6:n.2484C>G
ENST00000497377.6:n.2391C>G
ENST00000640094.2:c.895+116C>G	ENSP00000491275.2:n.895+116C>G
ENST00000696558.1:c.987C>G	ENSP00000512716.1:n.987C>G
ENST00000696559.1:c.918C>G	ENSP00000512717.1:p.Val306=
ENST00000696560.1:c.918C>G	ENSP00000512718.1:p.Val306=
ENST00000696561.1:c.918C>G	ENSP00000512719.1:p.Val306=
ENST00000696562.1:c.918C>G	ENSP00000512720.1:p.Val306=
ENST00000412585.7:c.918C>G MANE Select	ENSP00000399168.2:p.Val306=
ENST00000640094.1:c.88+116C>G	ENSP00000491275.1:n.88+116C>G
ENST00000412585.6:c.918C>G	ENSP00000399168.2:p.Val306=
ENST00000463574.1:n.509C>G
NM_005514.6:c.918C>G	NP_005505.2:p.Val306=
XM_011514556.1:c.951C>G	XP_011512858.1:p.Val317=
XM_011514557.1:c.895+116C>G	XP_011512859.1:n.895+116C>G
XR_926175.1:n.1357C>G
NM_005514.7:c.918C>G	NP_005505.2:p.Val306=
NM_005514.8:c.918C>G MANE Select	NP_005505.2:p.Val306=