Canonical Allele Identifier: CA1818335435

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343225G= , CM000670.2:g.127343225G= GRCh38
NC_000008.10:g.128355471G= , CM000670.1:g.128355471G= GRCh37
NC_000008.9:g.128424653G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-560+3790G= (POU5F1B) ENSP00000495779.1:n.-560+3790G=
NR_117099.1:n.457+3790G= (CASC21)
NR_117100.1:n.1177-53165C= (CASC8)