Canonical Allele Identifier: CA847153579

Linked Data

dbSNP Id: rs1449164541

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400806A>G , CM000670.2:g.127400806A>G GRCh38
NC_000008.10:g.128413051A>G , CM000670.1:g.128413051A>G GRCh37
NC_000008.9:g.128482233A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-14082A>G (POU5F1B) ENSP00000495779.1:n.-559-14082A>G
NR_109834.1:n.408A>G (CCAT2)
NR_117100.1:n.1176+20023T>C (CASC8)