Canonical Allele Identifier: CA1818352468

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401156T= , CM000670.2:g.127401156T= GRCh38
NC_000008.10:g.128413401T= , CM000670.1:g.128413401T= GRCh37
NC_000008.9:g.128482583T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13732T= (POU5F1B) ENSP00000495779.1:n.-559-13732T=
NR_109834.1:n.758T= (CCAT2)
NR_117100.1:n.1176+19673A= (CASC8)