Canonical Allele Identifier: CA1118993982

Linked Data

dbSNP Id: rs1814932560

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401037C>T , CM000670.2:g.127401037C>T GRCh38
NC_000008.10:g.128413282C>T , CM000670.1:g.128413282C>T GRCh37
NC_000008.9:g.128482464C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13851C>T (POU5F1B) ENSP00000495779.1:n.-559-13851C>T
NR_109834.1:n.639C>T (CCAT2)
NR_117100.1:n.1176+19792G>A (CASC8)