Canonical Allele Identifier: CA449603477
Gene: HLA-B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31325319A>G (hg19)

Genomic Alleles

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

Transcript Alleles

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