Canonical Allele Identifier: CA566689327

Gene: HLA-B

Linked Data

• dbSNP Id: rs1346326173
• gnomAD v2: 6-31322380-C-G
• gnomAD v4: 6-31354603-C-G
• MyVariant Identifiers: chr6:g.31322380C>G (hg19) ; chr6:g.31354603C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354603C>G , CM000668.2:g.31354603C>G	GRCh38
NC_000006.11:g.31322380C>G , CM000668.1:g.31322380C>G	GRCh37
NC_000006.10:g.31430359C>G	NCBI36
NG_023187.1:g.7610G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3092+30G>C
ENST00000481849.6:n.3052+30G>C
ENST00000497377.6:n.2959+30G>C
ENST00000640094.2:c.928+30G>C	ENSP00000491275.2:n.928+30G>C
ENST00000696558.1:c.1114+30G>C	ENSP00000512716.1:n.1114+30G>C
ENST00000696559.1:c.1045+30G>C	ENSP00000512717.1:n.1045+30G>C
ENST00000696560.1:c.1045+30G>C	ENSP00000512718.1:n.1045+30G>C
ENST00000696561.1:c.1045+30G>C	ENSP00000512719.1:n.1045+30G>C
ENST00000696562.1:c.1045+30G>C	ENSP00000512720.1:n.1045+30G>C
ENST00000412585.7:c.1045+30G>C MANE Select	ENSP00000399168.2:n.1045+30G>C
ENST00000640094.1:c.121+30G>C	ENSP00000491275.1:n.121+30G>C
ENST00000412585.6:c.1045+30G>C	ENSP00000399168.2:n.1045+30G>C
ENST00000481849.5:n.204G>C
ENST00000497377.5:n.444+30G>C
NM_005514.6:c.1045+30G>C	NP_005505.2:n.1045+30G>C
XM_011514556.1:c.1078+30G>C	XP_011512858.1:n.1078+30G>C
XM_011514557.1:c.928+30G>C	XP_011512859.1:n.928+30G>C
XR_926175.1:n.1484+30G>C
NM_005514.7:c.1045+30G>C	NP_005505.2:n.1045+30G>C
NM_005514.8:c.1045+30G>C MANE Select	NP_005505.2:n.1045+30G>C