Canonical Allele Identifier: CA1818352431

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401130G= , CM000670.2:g.127401130G= GRCh38
NC_000008.10:g.128413375G= , CM000670.1:g.128413375G= GRCh37
NC_000008.9:g.128482557G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13758G= (POU5F1B) ENSP00000495779.1:n.-559-13758G=
NR_109834.1:n.732G= (CCAT2)
NR_117100.1:n.1176+19699C= (CASC8)