Canonical Allele Identifier: CA1818352655

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401354T= , CM000670.2:g.127401354T= GRCh38
NC_000008.10:g.128413599T= , CM000670.1:g.128413599T= GRCh37
NC_000008.9:g.128482781T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13534T= (POU5F1B) ENSP00000495779.1:n.-559-13534T=
NR_109834.1:n.956T= (CCAT2)
NR_117100.1:n.1176+19475A= (CASC8)