Canonical Allele Identifier: CA2579837236

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400890C>A , CM000670.2:g.127400890C>A GRCh38
NC_000008.10:g.128413135C>A , CM000670.1:g.128413135C>A GRCh37
NC_000008.9:g.128482317C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13998C>A (POU5F1B) ENSP00000495779.1:n.-559-13998C>A
NR_109834.1:n.492C>A (CCAT2)
NR_117100.1:n.1176+19939G>T (CASC8)