Canonical Allele Identifier: CA1818335429

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343215T= , CM000670.2:g.127343215T= GRCh38
NC_000008.10:g.128355461T= , CM000670.1:g.128355461T= GRCh37
NC_000008.9:g.128424643T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-560+3780T= (POU5F1B) ENSP00000495779.1:n.-560+3780T=
NR_117099.1:n.457+3780T= (CASC21)
NR_117100.1:n.1177-53155A= (CASC8)