Canonical Allele Identifier: CA449790659

Gene: HLA-B

Linked Data

• dbSNP Id: rs1370323487
• gnomAD v4: 6-31355483-C-T
• MyVariant Identifiers: chr6:g.31323260C>T (hg19) ; chr6:g.31355483C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355483C>T , CM000668.2:g.31355483C>T	GRCh38
NC_000006.11:g.31323260C>T , CM000668.1:g.31323260C>T	GRCh37
NC_000006.10:g.31431239C>T	NCBI36
NG_023187.1:g.6730G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2776G>A
ENST00000481849.6:n.2202G>A
ENST00000497377.6:n.2202G>A
ENST00000640094.2:c.729G>A	ENSP00000491275.2:p.Arg243=
ENST00000696558.1:c.798G>A	ENSP00000512716.1:n.798G>A
ENST00000696559.1:c.729G>A	ENSP00000512717.1:p.Arg243=
ENST00000696560.1:c.729G>A	ENSP00000512718.1:p.Arg243=
ENST00000696561.1:c.729G>A	ENSP00000512719.1:p.Arg243=
ENST00000696562.1:c.729G>A	ENSP00000512720.1:p.Arg243=
ENST00000412585.7:c.729G>A MANE Select	ENSP00000399168.2:p.Arg243=
ENST00000412585.6:c.729G>A	ENSP00000399168.2:p.Arg243=
ENST00000463574.1:n.320G>A
ENST00000498007.1:n.995G>A
NM_005514.6:c.729G>A	NP_005505.2:p.Arg243=
XM_011514556.1:c.762G>A	XP_011512858.1:p.Arg254=
XM_011514557.1:c.729G>A	XP_011512859.1:p.Arg243=
XR_926175.1:n.1168G>A
NM_005514.7:c.729G>A	NP_005505.2:p.Arg243=
NM_005514.8:c.729G>A MANE Select	NP_005505.2:p.Arg243=