Canonical Allele Identifier: CA2688553327

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401520G>T , CM000670.2:g.127401520G>T GRCh38
NC_000008.10:g.128413765G>T , CM000670.1:g.128413765G>T GRCh37
NC_000008.9:g.128482947G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13368G>T (POU5F1B) ENSP00000495779.1:n.-559-13368G>T
NR_109834.1:n.1122G>T (CCAT2)
NR_117100.1:n.1176+19309C>A (CASC8)