Canonical Allele Identifier: CA1818319358

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127328634T= , CM000670.2:g.127328634T= GRCh38
NC_000008.10:g.128340879T= , CM000670.1:g.128340879T= GRCh37
NC_000008.9:g.128410061T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-715+6408T= (POU5F1B) ENSP00000495779.1:n.-715+6408T=
NR_117099.1:n.302+6408T= (CASC21)
NR_117100.1:n.1177-38574A= (CASC8)