Canonical Allele Identifier: CA1818352103

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400923_127400924delinsCT , CM000670.2:g.127400923_127400924delinsCT GRCh38
NC_000008.10:g.128413168_128413169delinsCT , CM000670.1:g.128413168_128413169delinsCT GRCh37
NC_000008.9:g.128482350_128482351delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13965_-559-13964delinsCT (POU5F1B) ENSP00000495779.1:n.-559-13965_-559-13964...
NR_109834.1:n.525_526delinsCT (CCAT2)
NR_117100.1:n.1176+19905_1176+19906delinsAG (CASC8)