Canonical Allele Identifier: CA363308595

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355133-G-C
• MyVariant Identifiers: chr6:g.31322910G>C (hg19) ; chr6:g.31355133G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355133G>C , CM000668.2:g.31355133G>C	GRCh38
NC_000006.11:g.31322910G>C , CM000668.1:g.31322910G>C	GRCh37
NC_000006.10:g.31430889G>C	NCBI36
NG_023187.1:g.7080C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3033C>G
ENST00000481849.6:n.2552C>G
ENST00000497377.6:n.2459C>G
ENST00000640094.2:c.895+184C>G	ENSP00000491275.2:n.895+184C>G
ENST00000696558.1:c.1055C>G	ENSP00000512716.1:n.1055C>G
ENST00000696559.1:c.986C>G	ENSP00000512717.1:p.Ala329Gly
ENST00000696560.1:c.986C>G	ENSP00000512718.1:p.Ala329Gly
ENST00000696561.1:c.986C>G	ENSP00000512719.1:p.Ala329Gly
ENST00000696562.1:c.986C>G	ENSP00000512720.1:p.Ala329Gly
ENST00000412585.7:c.986C>G MANE Select	ENSP00000399168.2:p.Ala329Gly
ENST00000640094.1:c.88+184C>G	ENSP00000491275.1:n.88+184C>G
ENST00000412585.6:c.986C>G	ENSP00000399168.2:p.Ala329Gly
ENST00000463574.1:n.577C>G
NM_005514.6:c.986C>G	NP_005505.2:p.Ala329Gly
XM_011514556.1:c.1019C>G	XP_011512858.1:p.Ala340Gly
XM_011514557.1:c.895+184C>G	XP_011512859.1:n.895+184C>G
XR_926175.1:n.1425C>G
NM_005514.7:c.986C>G	NP_005505.2:p.Ala329Gly
NM_005514.8:c.986C>G MANE Select	NP_005505.2:p.Ala329Gly