Canonical Allele Identifier: CA1818662082
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1813859604

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063572A>G , CM000670.2:g.128063572A>G GRCh38
NC_000008.10:g.129075818A>G , CM000670.1:g.129075818A>G GRCh37
NC_000008.9:g.129145000A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6588A>G