Canonical Allele Identifier: CA12426498
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs114443705
gnomAD v2: 6-31325317-C-T
gnomAD v3: 6-31357540-C-T
gnomAD v4: 6-31357540-C-T
MyVariant Identifiers: chr6:g.31325317C>T (hg19) chr6:g.31357540C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357540C>T , CM000668.2:g.31357540C>T GRCh38
NC_000006.11:g.31325317C>T , CM000668.1:g.31325317C>T GRCh37
NC_000006.10:g.31433296C>T NCBI36
NG_023187.1:g.4673G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1338+74G>A
ENST00000481849.6:n.1338+74G>A
ENST00000497377.6:n.1338+74G>A
ENST00000696559.1:c.-136+74G>A ENSP00000512717.1:n.-136+74G>A
ENST00000696560.1:c.-136+74G>A ENSP00000512718.1:n.-136+74G>A
ENST00000696561.1:c.-136+74G>A ENSP00000512719.1:n.-136+74G>A
ENST00000696562.1:c.-135-247G>A ENSP00000512720.1:n.-135-247G>A
ENST00000603274.1:n.894C>T
XR_926692.1:n.164+74G>A
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