Canonical Allele Identifier: CA2782146103
Gene: PVT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127802749C>A , CM000670.2:g.127802749C>A GRCh38
NC_000008.10:g.128814995C>A , CM000670.1:g.128814995C>A GRCh37
NC_000008.9:g.128884177C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.202+8015C>A