Canonical Allele Identifier: CA1818352206

Linked Data

dbSNP Id: rs1362283472

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401027C>T , CM000670.2:g.127401027C>T GRCh38
NC_000008.10:g.128413272C>T , CM000670.1:g.128413272C>T GRCh37
NC_000008.9:g.128482454C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13861C>T (POU5F1B) ENSP00000495779.1:n.-559-13861C>T
NR_109834.1:n.629C>T (CCAT2)
NR_117100.1:n.1176+19802G>A (CASC8)