Canonical Allele Identifier: CA1818352053

Linked Data

dbSNP Id: rs1586468272

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400875G>A , CM000670.2:g.127400875G>A GRCh38
NC_000008.10:g.128413120G>A , CM000670.1:g.128413120G>A GRCh37
NC_000008.9:g.128482302G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-14013G>A (POU5F1B) ENSP00000495779.1:n.-559-14013G>A
NR_109834.1:n.477G>A (CCAT2)
NR_117100.1:n.1176+19954C>T (CASC8)