Canonical Allele Identifier: CA1818319539

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127328810G= , CM000670.2:g.127328810G= GRCh38
NC_000008.10:g.128341055G= , CM000670.1:g.128341055G= GRCh37
NC_000008.9:g.128410237G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-715+6584G= (POU5F1B) ENSP00000495779.1:n.-715+6584G=
NR_117099.1:n.302+6584G= (CASC21)
NR_117100.1:n.1177-38750C= (CASC8)