Canonical Allele Identifier: CA363308704

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355149-C-G
• MyVariant Identifiers: chr6:g.31322926C>G (hg19) ; chr6:g.31355149C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355149C>G , CM000668.2:g.31355149C>G	GRCh38
NC_000006.11:g.31322926C>G , CM000668.1:g.31322926C>G	GRCh37
NC_000006.10:g.31430905C>G	NCBI36
NG_023187.1:g.7064G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3017G>C
ENST00000481849.6:n.2536G>C
ENST00000497377.6:n.2443G>C
ENST00000640094.2:c.895+168G>C	ENSP00000491275.2:n.895+168G>C
ENST00000696558.1:c.1039G>C	ENSP00000512716.1:n.1039G>C
ENST00000696559.1:c.970G>C	ENSP00000512717.1:p.Gly324Arg
ENST00000696560.1:c.970G>C	ENSP00000512718.1:p.Gly324Arg
ENST00000696561.1:c.970G>C	ENSP00000512719.1:p.Gly324Arg
ENST00000696562.1:c.970G>C	ENSP00000512720.1:p.Gly324Arg
ENST00000412585.7:c.970G>C MANE Select	ENSP00000399168.2:p.Gly324Arg
ENST00000640094.1:c.88+168G>C	ENSP00000491275.1:n.88+168G>C
ENST00000412585.6:c.970G>C	ENSP00000399168.2:p.Gly324Arg
ENST00000463574.1:n.561G>C
NM_005514.6:c.970G>C	NP_005505.2:p.Gly324Arg
XM_011514556.1:c.1003G>C	XP_011512858.1:p.Gly335Arg
XM_011514557.1:c.895+168G>C	XP_011512859.1:n.895+168G>C
XR_926175.1:n.1409G>C
NM_005514.7:c.970G>C	NP_005505.2:p.Gly324Arg
NM_005514.8:c.970G>C MANE Select	NP_005505.2:p.Gly324Arg