Canonical Allele Identifier: CA3711342

Gene: HLA-B

Linked Data

• ClinVar Variation Id: 3025081
• ClinVar RCV Id: RCV003885957
• dbSNP Id: rs1065502
• ExAC: 6:31323155 C / T
• gnomAD v2: 6-31323155-C-T
• gnomAD v3: 6-31355378-C-T
• gnomAD v4: 6-31355378-C-T
• MyVariant Identifiers: chr6:g.31323155C>T (hg19) ; chr6:g.31355378C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355378C>T , CM000668.2:g.31355378C>T	GRCh38
NC_000006.11:g.31323155C>T , CM000668.1:g.31323155C>T	GRCh37
NC_000006.10:g.31431134C>T	NCBI36
NG_023187.1:g.6835G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2881G>A
ENST00000481849.6:n.2307G>A
ENST00000497377.6:n.2307G>A
ENST00000640094.2:c.834G>A	ENSP00000491275.2:p.Glu278=
ENST00000696558.1:c.903G>A	ENSP00000512716.1:n.903G>A
ENST00000696559.1:c.834G>A	ENSP00000512717.1:p.Glu278=
ENST00000696560.1:c.834G>A	ENSP00000512718.1:p.Glu278=
ENST00000696561.1:c.834G>A	ENSP00000512719.1:p.Glu278=
ENST00000696562.1:c.834G>A	ENSP00000512720.1:p.Glu278=
ENST00000412585.7:c.834G>A MANE Select	ENSP00000399168.2:p.Glu278=
ENST00000640094.1:c.27G>A	ENSP00000491275.1:p.Glu9=
ENST00000412585.6:c.834G>A	ENSP00000399168.2:p.Glu278=
ENST00000463574.1:n.425G>A
NM_005514.6:c.834G>A	NP_005505.2:p.Glu278=
XM_011514556.1:c.867G>A	XP_011512858.1:p.Glu289=
XM_011514557.1:c.834G>A	XP_011512859.1:p.Glu278=
XR_926175.1:n.1273G>A
NM_005514.7:c.834G>A	NP_005505.2:p.Glu278=
NM_005514.8:c.834G>A MANE Select	NP_005505.2:p.Glu278=