Canonical Allele Identifier: CA2579836683

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400869G>T , CM000670.2:g.127400869G>T GRCh38
NC_000008.10:g.128413114G>T , CM000670.1:g.128413114G>T GRCh37
NC_000008.9:g.128482296G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-14019G>T (POU5F1B) ENSP00000495779.1:n.-559-14019G>T
NR_109834.1:n.471G>T (CCAT2)
NR_117100.1:n.1176+19960C>A (CASC8)