Canonical Allele Identifier: CA847153649

Linked Data

dbSNP Id: rs1349421462

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400995C>T , CM000670.2:g.127400995C>T GRCh38
NC_000008.10:g.128413240C>T , CM000670.1:g.128413240C>T GRCh37
NC_000008.9:g.128482422C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13893C>T (POU5F1B) ENSP00000495779.1:n.-559-13893C>T
NR_109834.1:n.597C>T (CCAT2)
NR_117100.1:n.1176+19834G>A (CASC8)