Canonical Allele Identifier: CA1119063752
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1813861205

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063663G>T , CM000670.2:g.128063663G>T GRCh38
NC_000008.10:g.129075909G>T , CM000670.1:g.129075909G>T GRCh37
NC_000008.9:g.129145091G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6497G>T