Canonical Allele Identifier: CA1818352024

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400837C= , CM000670.2:g.127400837C= GRCh38
NC_000008.10:g.128413082C= , CM000670.1:g.128413082C= GRCh37
NC_000008.9:g.128482264C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-14051C= (POU5F1B) ENSP00000495779.1:n.-559-14051C=
NR_109834.1:n.439C= (CCAT2)
NR_117100.1:n.1176+19992G= (CASC8)