Canonical Allele Identifier: CA449602946
Gene: HLA-B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31325254G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357477G>C , CM000668.2:g.31357477G>C GRCh38
NC_000006.11:g.31325254G>C , CM000668.1:g.31325254G>C GRCh37
NC_000006.10:g.31433233G>C NCBI36
NG_023187.1:g.4736C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1338+137C>G
ENST00000481849.6:n.1338+137C>G
ENST00000497377.6:n.1338+137C>G
ENST00000696559.1:c.-136+137C>G ENSP00000512717.1:n.-136+137C>G
ENST00000696560.1:c.-136+137C>G ENSP00000512718.1:n.-136+137C>G
ENST00000696561.1:c.-136+137C>G ENSP00000512719.1:n.-136+137C>G
ENST00000696562.1:c.-135-184C>G ENSP00000512720.1:n.-135-184C>G
ENST00000603274.1:n.831G>C
XR_926692.1:n.164+137C>G