Canonical Allele Identifier: CA1818352048

Linked Data

dbSNP Id: rs1814930238

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400869G>A , CM000670.2:g.127400869G>A GRCh38
NC_000008.10:g.128413114G>A , CM000670.1:g.128413114G>A GRCh37
NC_000008.9:g.128482296G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-14019G>A (POU5F1B) ENSP00000495779.1:n.-559-14019G>A
NR_109834.1:n.471G>A (CCAT2)
NR_117100.1:n.1176+19960C>T (CASC8)