Canonical Allele Identifier: CA1818319372

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127328651A= , CM000670.2:g.127328651A= GRCh38
NC_000008.10:g.128340896A= , CM000670.1:g.128340896A= GRCh37
NC_000008.9:g.128410078A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-715+6425A= (POU5F1B) ENSP00000495779.1:n.-715+6425A=
NR_117099.1:n.302+6425A= (CASC21)
NR_117100.1:n.1177-38591T= (CASC8)