Canonical Allele Identifier: CA449603845

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357601-T-G
• MyVariant Identifiers: chr6:g.31325378T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357601T>G , CM000668.2:g.31357601T>G	GRCh38
NC_000006.11:g.31325378T>G , CM000668.1:g.31325378T>G	GRCh37
NC_000006.10:g.31433357T>G	NCBI36
NG_023187.1:g.4612A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1338+13A>C
ENST00000481849.6:n.1338+13A>C
ENST00000497377.6:n.1338+13A>C
ENST00000696559.1:c.-136+13A>C	ENSP00000512717.1:n.-136+13A>C
ENST00000696560.1:c.-136+13A>C	ENSP00000512718.1:n.-136+13A>C
ENST00000696561.1:c.-136+13A>C	ENSP00000512719.1:n.-136+13A>C
ENST00000696562.1:c.-135-308A>C	ENSP00000512720.1:n.-135-308A>C
ENST00000603274.1:n.955T>G
XR_926692.1:n.164+13A>C