Canonical Allele Identifier: CA449603850

Gene: HLA-B

Linked Data

• dbSNP Id: rs9266231
• gnomAD v4: 6-31357603-C-G
• MyVariant Identifiers: chr6:g.31325380C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357603C>G , CM000668.2:g.31357603C>G	GRCh38
NC_000006.11:g.31325380C>G , CM000668.1:g.31325380C>G	GRCh37
NC_000006.10:g.31433359C>G	NCBI36
NG_023187.1:g.4610G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1338+11G>C
ENST00000481849.6:n.1338+11G>C
ENST00000497377.6:n.1338+11G>C
ENST00000696559.1:c.-136+11G>C	ENSP00000512717.1:n.-136+11G>C
ENST00000696560.1:c.-136+11G>C	ENSP00000512718.1:n.-136+11G>C
ENST00000696561.1:c.-136+11G>C	ENSP00000512719.1:n.-136+11G>C
ENST00000696562.1:c.-135-310G>C	ENSP00000512720.1:n.-135-310G>C
ENST00000603274.1:n.957C>G
XR_926692.1:n.164+11G>C