Canonical Allele Identifier: CA1818661899
Gene: PVT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063467G= , CM000670.2:g.128063467G= GRCh38
NC_000008.10:g.129075713G= , CM000670.1:g.129075713G= GRCh37
NC_000008.9:g.129144895G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6693G=