Canonical Allele Identifier: CA847160767

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343315_127343316insAG , CM000670.2:g.127343315_127343316insAG GRCh38
NC_000008.10:g.128355561_128355562insAG , CM000670.1:g.128355561_128355562insAG GRCh37
NC_000008.9:g.128424743_128424744insAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-560+3880_-560+3881insAG (POU5F1B) ENSP00000495779.1:n.-560+3880_-560+3881insAG
NR_117099.1:n.457+3880_457+3881insAG (CASC21)
NR_117100.1:n.1177-53256_1177-53255insCT (CASC8)