Canonical Allele Identifier: CA449791307
Gene: HLA-B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31325108G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357331G>A , CM000668.2:g.31357331G>A GRCh38
NC_000006.11:g.31325108G>A , CM000668.1:g.31325108G>A GRCh37
NC_000006.10:g.31433087G>A NCBI36
NG_023187.1:g.4882C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1339-38C>T
ENST00000481849.6:n.1339-38C>T
ENST00000497377.6:n.1339-38C>T
ENST00000696559.1:c.-135-38C>T ENSP00000512717.1:n.-135-38C>T
ENST00000696560.1:c.-135-38C>T ENSP00000512718.1:n.-135-38C>T
ENST00000696561.1:c.-135-38C>T ENSP00000512719.1:n.-135-38C>T
ENST00000696562.1:c.-135-38C>T ENSP00000512720.1:n.-135-38C>T
ENST00000603274.1:n.685G>A
XR_926692.1:n.165-38C>T
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