Canonical Allele Identifier: CA847153916

Linked Data

dbSNP Id: rs1463325386

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401342G>A , CM000670.2:g.127401342G>A GRCh38
NC_000008.10:g.128413587G>A , CM000670.1:g.128413587G>A GRCh37
NC_000008.9:g.128482769G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13546G>A (POU5F1B) ENSP00000495779.1:n.-559-13546G>A
NR_109834.1:n.944G>A (CCAT2)
NR_117100.1:n.1176+19487C>T (CASC8)