Canonical Allele Identifier: CA2579837227

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400887T>A , CM000670.2:g.127400887T>A GRCh38
NC_000008.10:g.128413132T>A , CM000670.1:g.128413132T>A GRCh37
NC_000008.9:g.128482314T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-14001T>A (POU5F1B) ENSP00000495779.1:n.-559-14001T>A
NR_109834.1:n.489T>A (CCAT2)
NR_117100.1:n.1176+19942A>T (CASC8)