Canonical Allele Identifier: CA2579837898

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401113A>C , CM000670.2:g.127401113A>C GRCh38
NC_000008.10:g.128413358A>C , CM000670.1:g.128413358A>C GRCh37
NC_000008.9:g.128482540A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13775A>C (POU5F1B) ENSP00000495779.1:n.-559-13775A>C
NR_109834.1:n.715A>C (CCAT2)
NR_117100.1:n.1176+19716T>G (CASC8)