Canonical Allele Identifier: CA1818352821

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401504G= , CM000670.2:g.127401504G= GRCh38
NC_000008.10:g.128413749G= , CM000670.1:g.128413749G= GRCh37
NC_000008.9:g.128482931G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13384G= (POU5F1B) ENSP00000495779.1:n.-559-13384G=
NR_109834.1:n.1106G= (CCAT2)
NR_117100.1:n.1176+19325C= (CASC8)