Canonical Allele Identifier: CA136836840

Gene: HLA-B

Linked Data

• dbSNP Id: rs1040851094
• gnomAD v4: 6-31357542-A-C
• MyVariant Identifiers: chr6:g.31325319A>C (hg19) ; chr6:g.31357542A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357542A>C , CM000668.2:g.31357542A>C	GRCh38
NC_000006.11:g.31325319A>C , CM000668.1:g.31325319A>C	GRCh37
NC_000006.10:g.31433298A>C	NCBI36
NG_023187.1:g.4671T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1338+72T>G
ENST00000481849.6:n.1338+72T>G
ENST00000497377.6:n.1338+72T>G
ENST00000696559.1:c.-136+72T>G	ENSP00000512717.1:n.-136+72T>G
ENST00000696560.1:c.-136+72T>G	ENSP00000512718.1:n.-136+72T>G
ENST00000696561.1:c.-136+72T>G	ENSP00000512719.1:n.-136+72T>G
ENST00000696562.1:c.-135-249T>G	ENSP00000512720.1:n.-135-249T>G
ENST00000603274.1:n.896A>C
XR_926692.1:n.164+72T>G