Canonical Allele Identifier: CA1818529867
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1814480247

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127802787C>T , CM000670.2:g.127802787C>T GRCh38
NC_000008.10:g.128815033C>T , CM000670.1:g.128815033C>T GRCh37
NC_000008.9:g.128884215C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.202+8053C>T