Canonical Allele Identifier: CA449603879
Gene: HLA-B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31325390C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357613C>G , CM000668.2:g.31357613C>G GRCh38
NC_000006.11:g.31325390C>G , CM000668.1:g.31325390C>G GRCh37
NC_000006.10:g.31433369C>G NCBI36
NG_023187.1:g.4600G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1338+1G>C
ENST00000481849.6:n.1338+1G>C
ENST00000497377.6:n.1338+1G>C
ENST00000696559.1:c.-136+1G>C ENSP00000512717.1:n.-136+1G>C
ENST00000696560.1:c.-136+1G>C ENSP00000512718.1:n.-136+1G>C
ENST00000696561.1:c.-136+1G>C ENSP00000512719.1:n.-136+1G>C
ENST00000696562.1:c.-135-320G>C ENSP00000512720.1:n.-135-320G>C
ENST00000603274.1:n.967C>G
XR_926692.1:n.164+1G>C
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