Canonical Allele Identifier: CA449790746

Gene: HLA-B

Linked Data

• dbSNP Id: rs9266141
• gnomAD v3: 6-31356246-C-A
• gnomAD v4: 6-31356246-C-A
• MyVariant Identifiers: chr6:g.31324023C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356246C>A , CM000668.2:g.31356246C>A	GRCh38
NC_000006.11:g.31324023C>A , CM000668.1:g.31324023C>A	GRCh37
NC_000006.10:g.31432002C>A	NCBI36
NG_023187.1:g.5967G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2013G>T
ENST00000481849.6:n.2013G>T
ENST00000497377.6:n.2013G>T
ENST00000640094.2:c.540G>T	ENSP00000491275.2:p.Arg180=
ENST00000696558.1:c.540G>T	ENSP00000512716.1:p.Arg180=
ENST00000696559.1:c.540G>T	ENSP00000512717.1:p.Arg180=
ENST00000696560.1:c.540G>T	ENSP00000512718.1:p.Arg180=
ENST00000696561.1:c.540G>T	ENSP00000512719.1:p.Arg180=
ENST00000696562.1:c.540G>T	ENSP00000512720.1:p.Arg180=
ENST00000412585.7:c.540G>T MANE Select	ENSP00000399168.2:p.Arg180=
ENST00000412585.6:c.540G>T	ENSP00000399168.2:p.Arg180=
ENST00000434333.1:c.573G>T	ENSP00000405931.1:p.Arg191=
ENST00000474381.1:n.415G>T
ENST00000498007.1:n.806G>T
NM_005514.6:c.540G>T	NP_005505.2:p.Arg180=
XM_011514556.1:c.573G>T	XP_011512858.1:p.Arg191=
XM_011514557.1:c.540G>T	XP_011512859.1:p.Arg180=
XR_926175.1:n.550G>T
NM_005514.7:c.540G>T	NP_005505.2:p.Arg180=
NM_005514.8:c.540G>T MANE Select	NP_005505.2:p.Arg180=