Canonical Allele Identifier: CA847202494
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1289722155

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127802815del , CM000670.2:g.127802815del GRCh38
NC_000008.10:g.128815061del , CM000670.1:g.128815061del GRCh37
NC_000008.9:g.128884243del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.202+8081del