Canonical Allele Identifier: CA2677958302
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357547_31357548insGG , CM000668.2:g.31357547_31357548insGG GRCh38
NC_000006.11:g.31325324_31325325insGG , CM000668.1:g.31325324_31325325insGG GRCh37
NC_000006.10:g.31433303_31433304insGG NCBI36
NG_023187.1:g.4665_4666insCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1338+66_1338+67insCC
ENST00000481849.6:n.1338+66_1338+67insCC
ENST00000497377.6:n.1338+66_1338+67insCC
ENST00000696559.1:c.-136+66_-136+67insCC ENSP00000512717.1:n.-136+66_-136+67insCC
ENST00000696560.1:c.-136+66_-136+67insCC ENSP00000512718.1:n.-136+66_-136+67insCC
ENST00000696561.1:c.-136+66_-136+67insCC ENSP00000512719.1:n.-136+66_-136+67insCC
ENST00000696562.1:c.-135-255_-135-254insCC ENSP00000512720.1:n.-135-255_-135-254insCC
ENST00000603274.1:n.901_902insGG
XR_926692.1:n.164+66_164+67insCC