Canonical Allele Identifier: CA1818352057

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400882T= , CM000670.2:g.127400882T= GRCh38
NC_000008.10:g.128413127T= , CM000670.1:g.128413127T= GRCh37
NC_000008.9:g.128482309T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-14006T= (POU5F1B) ENSP00000495779.1:n.-559-14006T=
NR_109834.1:n.484T= (CCAT2)
NR_117100.1:n.1176+19947A= (CASC8)