Canonical Allele Identifier: CA136836857
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs549333654
gnomAD v3: 6-31357614-C-A
gnomAD v4: 6-31357614-C-A
MyVariant Identifiers: chr6:g.31325391C>A (hg19) chr6:g.31357614C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357614C>A , CM000668.2:g.31357614C>A GRCh38
NC_000006.11:g.31325391C>A , CM000668.1:g.31325391C>A GRCh37
NC_000006.10:g.31433370C>A NCBI36
NG_023187.1:g.4599G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1338G>T
ENST00000481849.6:n.1338G>T
ENST00000497377.6:n.1338G>T
ENST00000696559.1:c.-136G>T ENSP00000512717.1:n.-136G>T
ENST00000696560.1:c.-136G>T ENSP00000512718.1:n.-136G>T
ENST00000696561.1:c.-136G>T ENSP00000512719.1:n.-136G>T
ENST00000696562.1:c.-135-321G>T ENSP00000512720.1:n.-135-321G>T
ENST00000603274.1:n.968C>A
XR_926692.1:n.164G>T
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