Canonical Allele Identifier: CA2579837707

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401052G>C , CM000670.2:g.127401052G>C GRCh38
NC_000008.10:g.128413297G>C , CM000670.1:g.128413297G>C GRCh37
NC_000008.9:g.128482479G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13836G>C (POU5F1B) ENSP00000495779.1:n.-559-13836G>C
NR_109834.1:n.654G>C (CCAT2)
NR_117100.1:n.1176+19777C>G (CASC8)