Canonical Allele Identifier: CA1818335558

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343322T= , CM000670.2:g.127343322T= GRCh38
NC_000008.10:g.128355568T= , CM000670.1:g.128355568T= GRCh37
NC_000008.9:g.128424750T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-560+3887T= (POU5F1B) ENSP00000495779.1:n.-560+3887T=
NR_117099.1:n.457+3887T= (CASC21)
NR_117100.1:n.1177-53262A= (CASC8)