Canonical Allele Identifier: CA2579837269

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400902C>A , CM000670.2:g.127400902C>A GRCh38
NC_000008.10:g.128413147C>A , CM000670.1:g.128413147C>A GRCh37
NC_000008.9:g.128482329C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13986C>A (POU5F1B) ENSP00000495779.1:n.-559-13986C>A
NR_109834.1:n.504C>A (CCAT2)
NR_117100.1:n.1176+19927G>T (CASC8)