Canonical Allele Identifier: CA363308425

Gene: HLA-B

Linked Data

• dbSNP Id: rs1476457470
• gnomAD v3: 6-31355105-A-C
• gnomAD v4: 6-31355105-A-C
• MyVariant Identifiers: chr6:g.31322882A>C (hg19) ; chr6:g.31355105A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355105A>C , CM000668.2:g.31355105A>C	GRCh38
NC_000006.11:g.31322882A>C , CM000668.1:g.31322882A>C	GRCh37
NC_000006.10:g.31430861A>C	NCBI36
NG_023187.1:g.7108T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+2T>G
ENST00000481849.6:n.2580T>G
ENST00000497377.6:n.2487T>G
ENST00000640094.2:c.895+212T>G	ENSP00000491275.2:n.895+212T>G
ENST00000696558.1:c.1081+2T>G	ENSP00000512716.1:n.1081+2T>G
ENST00000696559.1:c.1012+2T>G	ENSP00000512717.1:n.1012+2T>G
ENST00000696560.1:c.1012+2T>G	ENSP00000512718.1:n.1012+2T>G
ENST00000696561.1:c.1012+2T>G	ENSP00000512719.1:n.1012+2T>G
ENST00000696562.1:c.1012+2T>G	ENSP00000512720.1:n.1012+2T>G
ENST00000412585.7:c.1012+2T>G MANE Select	ENSP00000399168.2:n.1012+2T>G
ENST00000640094.1:c.88+212T>G	ENSP00000491275.1:n.88+212T>G
ENST00000412585.6:c.1012+2T>G	ENSP00000399168.2:n.1012+2T>G
NM_005514.6:c.1012+2T>G	NP_005505.2:n.1012+2T>G
XM_011514556.1:c.1045+2T>G	XP_011512858.1:n.1045+2T>G
XM_011514557.1:c.895+212T>G	XP_011512859.1:n.895+212T>G
XR_926175.1:n.1451+2T>G
NM_005514.7:c.1012+2T>G	NP_005505.2:n.1012+2T>G
NM_005514.8:c.1012+2T>G MANE Select	NP_005505.2:n.1012+2T>G