Canonical Allele Identifier: CA1818351989

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400806A= , CM000670.2:g.127400806A= GRCh38
NC_000008.10:g.128413051A= , CM000670.1:g.128413051A= GRCh37
NC_000008.9:g.128482233A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-14082A= (POU5F1B) ENSP00000495779.1:n.-559-14082A=
NR_109834.1:n.408A= (CCAT2)
NR_117100.1:n.1176+20023T= (CASC8)