Canonical Allele Identifier: CA1818335569

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343326A= , CM000670.2:g.127343326A= GRCh38
NC_000008.10:g.128355572A= , CM000670.1:g.128355572A= GRCh37
NC_000008.9:g.128424754A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-560+3891A= (POU5F1B) ENSP00000495779.1:n.-560+3891A=
NR_117099.1:n.457+3891A= (CASC21)
NR_117100.1:n.1177-53266T= (CASC8)