Canonical Allele Identifier: CA1818661845
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1813856780

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063419C>A , CM000670.2:g.128063419C>A GRCh38
NC_000008.10:g.129075665C>A , CM000670.1:g.129075665C>A GRCh37
NC_000008.9:g.129144847C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6741C>A