Canonical Allele Identifier: CA585068472

Linked Data

dbSNP Id: rs1026716232

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401015C>A , CM000670.2:g.127401015C>A GRCh38
NC_000008.10:g.128413260C>A , CM000670.1:g.128413260C>A GRCh37
NC_000008.9:g.128482442C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13873C>A (POU5F1B) ENSP00000495779.1:n.-559-13873C>A
NR_109834.1:n.617C>A (CCAT2)
NR_117100.1:n.1176+19814G>T (CASC8)