Canonical Allele Identifier: CA1818661897
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1813857313

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063461del , CM000670.2:g.128063461del GRCh38
NC_000008.10:g.129075707del , CM000670.1:g.129075707del GRCh37
NC_000008.9:g.129144889del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6699del