Canonical Allele Identifier: CA1818319503

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127328764C= , CM000670.2:g.127328764C= GRCh38
NC_000008.10:g.128341009C= , CM000670.1:g.128341009C= GRCh37
NC_000008.9:g.128410191C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-715+6538C= (POU5F1B) ENSP00000495779.1:n.-715+6538C=
NR_117099.1:n.302+6538C= (CASC21)
NR_117100.1:n.1177-38704G= (CASC8)