Canonical Allele Identifier: CA1087445352
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1767226567
gnomAD v3: 6-31357373-A-AACGC
gnomAD v4: 6-31357373-A-AACGC
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357373_31357374insACGC , CM000668.2:g.31357373_31357374insACGC GRCh38
NC_000006.11:g.31325150_31325151insACGC , CM000668.1:g.31325150_31325151insACGC GRCh37
NC_000006.10:g.31433129_31433130insACGC NCBI36
NG_023187.1:g.4839_4840insGCGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1339-81_1339-80insGCGT
ENST00000481849.6:n.1339-81_1339-80insGCGT
ENST00000497377.6:n.1339-81_1339-80insGCGT
ENST00000696559.1:c.-135-81_-135-80insGCGT ENSP00000512717.1:n.-135-81_-135-80insGCGT
ENST00000696560.1:c.-135-81_-135-80insGCGT ENSP00000512718.1:n.-135-81_-135-80insGCGT
ENST00000696561.1:c.-135-81_-135-80insGCGT ENSP00000512719.1:n.-135-81_-135-80insGCGT
ENST00000696562.1:c.-135-81_-135-80insGCGT ENSP00000512720.1:n.-135-81_-135-80insGCGT
ENST00000603274.1:n.727_728insACGC
XR_926692.1:n.165-81_165-80insGCGT
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