Canonical Allele Identifier: CA847153645

Linked Data

dbSNP Id: rs1328256081

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400980C>T , CM000670.2:g.127400980C>T GRCh38
NC_000008.10:g.128413225C>T , CM000670.1:g.128413225C>T GRCh37
NC_000008.9:g.128482407C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13908C>T (POU5F1B) ENSP00000495779.1:n.-559-13908C>T
NR_109834.1:n.582C>T (CCAT2)
NR_117100.1:n.1176+19849G>A (CASC8)