Canonical Allele Identifier: CA1118994167

Linked Data

dbSNP Id: rs1010211271

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401491G>T , CM000670.2:g.127401491G>T GRCh38
NC_000008.10:g.128413736G>T , CM000670.1:g.128413736G>T GRCh37
NC_000008.9:g.128482918G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13397G>T (POU5F1B) ENSP00000495779.1:n.-559-13397G>T
NR_109834.1:n.1093G>T (CCAT2)
NR_117100.1:n.1176+19338C>A (CASC8)