Canonical Allele Identifier: CA1818352161

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400991T= , CM000670.2:g.127400991T= GRCh38
NC_000008.10:g.128413236T= , CM000670.1:g.128413236T= GRCh37
NC_000008.9:g.128482418T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13897T= (POU5F1B) ENSP00000495779.1:n.-559-13897T=
NR_109834.1:n.593T= (CCAT2)
NR_117100.1:n.1176+19838A= (CASC8)