Canonical Allele Identifier: CA1818352050

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400873T= , CM000670.2:g.127400873T= GRCh38
NC_000008.10:g.128413118T= , CM000670.1:g.128413118T= GRCh37
NC_000008.9:g.128482300T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-14015T= (POU5F1B) ENSP00000495779.1:n.-559-14015T=
NR_109834.1:n.475T= (CCAT2)
NR_117100.1:n.1176+19956A= (CASC8)