Canonical Allele Identifier: CA2782153615
Gene: PVT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063565C>A , CM000670.2:g.128063565C>A GRCh38
NC_000008.10:g.129075811C>A , CM000670.1:g.129075811C>A GRCh37
NC_000008.9:g.129144993C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6595C>A