Canonical Allele Identifier: CA449790757

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356279-G-C
• MyVariant Identifiers: chr6:g.31324056G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356279G>C , CM000668.2:g.31356279G>C	GRCh38
NC_000006.11:g.31324056G>C , CM000668.1:g.31324056G>C	GRCh37
NC_000006.10:g.31432035G>C	NCBI36
NG_023187.1:g.5934C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1980C>G
ENST00000481849.6:n.1980C>G
ENST00000497377.6:n.1980C>G
ENST00000640094.2:c.507C>G	ENSP00000491275.2:p.Arg169=
ENST00000696558.1:c.507C>G	ENSP00000512716.1:p.Arg169=
ENST00000696559.1:c.507C>G	ENSP00000512717.1:p.Arg169=
ENST00000696560.1:c.507C>G	ENSP00000512718.1:p.Arg169=
ENST00000696561.1:c.507C>G	ENSP00000512719.1:p.Arg169=
ENST00000696562.1:c.507C>G	ENSP00000512720.1:p.Arg169=
ENST00000412585.7:c.507C>G MANE Select	ENSP00000399168.2:p.Arg169=
ENST00000412585.6:c.507C>G	ENSP00000399168.2:p.Arg169=
ENST00000434333.1:c.540C>G	ENSP00000405931.1:p.Arg180=
ENST00000474381.1:n.382C>G
ENST00000498007.1:n.773C>G
NM_005514.6:c.507C>G	NP_005505.2:p.Arg169=
XM_011514556.1:c.540C>G	XP_011512858.1:p.Arg180=
XM_011514557.1:c.507C>G	XP_011512859.1:p.Arg169=
XR_926175.1:n.517C>G
NM_005514.7:c.507C>G	NP_005505.2:p.Arg169=
NM_005514.8:c.507C>G MANE Select	NP_005505.2:p.Arg169=