Canonical Allele Identifier: CA2579837498

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400979A>C , CM000670.2:g.127400979A>C GRCh38
NC_000008.10:g.128413224A>C , CM000670.1:g.128413224A>C GRCh37
NC_000008.9:g.128482406A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13909A>C (POU5F1B) ENSP00000495779.1:n.-559-13909A>C
NR_109834.1:n.581A>C (CCAT2)
NR_117100.1:n.1176+19850T>G (CASC8)