Canonical Allele Identifier: CA1818319424

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127328707A= , CM000670.2:g.127328707A= GRCh38
NC_000008.10:g.128340952A= , CM000670.1:g.128340952A= GRCh37
NC_000008.9:g.128410134A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-715+6481A= (POU5F1B) ENSP00000495779.1:n.-715+6481A=
NR_117099.1:n.302+6481A= (CASC21)
NR_117100.1:n.1177-38647T= (CASC8)