Canonical Allele Identifier: CA1818352494

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401186C= , CM000670.2:g.127401186C= GRCh38
NC_000008.10:g.128413431C= , CM000670.1:g.128413431C= GRCh37
NC_000008.9:g.128482613C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13702C= (POU5F1B) ENSP00000495779.1:n.-559-13702C=
NR_109834.1:n.788C= (CCAT2)
NR_117100.1:n.1176+19643G= (CASC8)