Canonical Allele Identifier: CA1818319416

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127328697T= , CM000670.2:g.127328697T= GRCh38
NC_000008.10:g.128340942T= , CM000670.1:g.128340942T= GRCh37
NC_000008.9:g.128410124T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-715+6471T= (POU5F1B) ENSP00000495779.1:n.-715+6471T=
NR_117099.1:n.302+6471T= (CASC21)
NR_117100.1:n.1177-38637A= (CASC8)