Canonical Allele Identifier: CA2579836854

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401306T= , CM000670.2:g.127401306T= GRCh38
NC_000008.10:g.128413551T= , CM000670.1:g.128413551T= GRCh37
NC_000008.9:g.128482733T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13582T= (POU5F1B) ENSP00000495779.1:n.-559-13582T=
NR_109834.1:n.908T= (CCAT2)
NR_117100.1:n.1176+19523A= (CASC8)