Canonical Allele Identifier: CA1818319435

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127328723T= , CM000670.2:g.127328723T= GRCh38
NC_000008.10:g.128340968T= , CM000670.1:g.128340968T= GRCh37
NC_000008.9:g.128410150T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-715+6497T= (POU5F1B) ENSP00000495779.1:n.-715+6497T=
NR_117099.1:n.302+6497T= (CASC21)
NR_117100.1:n.1177-38663A= (CASC8)