Canonical Allele Identifier: CA1818352753

Linked Data

dbSNP Id: rs1586468548

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401429A>T , CM000670.2:g.127401429A>T GRCh38
NC_000008.10:g.128413674A>T , CM000670.1:g.128413674A>T GRCh37
NC_000008.9:g.128482856A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13459A>T (POU5F1B) ENSP00000495779.1:n.-559-13459A>T
NR_109834.1:n.1031A>T (CCAT2)
NR_117100.1:n.1176+19400T>A (CASC8)