Canonical Allele Identifier: CA449603918
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1582562207
MyVariant Identifiers: chr6:g.31325404C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357627C>A , CM000668.2:g.31357627C>A GRCh38
NC_000006.11:g.31325404C>A , CM000668.1:g.31325404C>A GRCh37
NC_000006.10:g.31433383C>A NCBI36
NG_023187.1:g.4586G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1325G>T
ENST00000481849.6:n.1325G>T
ENST00000497377.6:n.1325G>T
ENST00000696559.1:c.-149G>T ENSP00000512717.1:n.-149G>T
ENST00000696560.1:c.-149G>T ENSP00000512718.1:n.-149G>T
ENST00000696561.1:c.-149G>T ENSP00000512719.1:n.-149G>T
ENST00000696562.1:c.-135-334G>T ENSP00000512720.1:n.-135-334G>T
ENST00000603274.1:n.981C>A
XR_926692.1:n.151G>T
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