Canonical Allele Identifier: CA1818352830

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401522C= , CM000670.2:g.127401522C= GRCh38
NC_000008.10:g.128413767C= , CM000670.1:g.128413767C= GRCh37
NC_000008.9:g.128482949C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13366C= (POU5F1B) ENSP00000495779.1:n.-559-13366C=
NR_109834.1:n.1124C= (CCAT2)
NR_117100.1:n.1176+19307G= (CASC8)