Canonical Allele Identifier: CA1818335419

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343190C= , CM000670.2:g.127343190C= GRCh38
NC_000008.10:g.128355436C= , CM000670.1:g.128355436C= GRCh37
NC_000008.9:g.128424618C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-560+3755C= (POU5F1B) ENSP00000495779.1:n.-560+3755C=
NR_117099.1:n.457+3755C= (CASC21)
NR_117100.1:n.1177-53130G= (CASC8)