Canonical Allele Identifier: CA585068471

Linked Data

dbSNP Id: rs1164910835

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400976G>A , CM000670.2:g.127400976G>A GRCh38
NC_000008.10:g.128413221G>A , CM000670.1:g.128413221G>A GRCh37
NC_000008.9:g.128482403G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13912G>A (POU5F1B) ENSP00000495779.1:n.-559-13912G>A
NR_109834.1:n.578G>A (CCAT2)
NR_117100.1:n.1176+19853C>T (CASC8)