Canonical Allele Identifier: CA1818662304
Gene: PVT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063716G= , CM000670.2:g.128063716G= GRCh38
NC_000008.10:g.129075962G= , CM000670.1:g.129075962G= GRCh37
NC_000008.9:g.129145144G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6444G=