Canonical Allele Identifier: CA1818662286
Gene: PVT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063688G= , CM000670.2:g.128063688G= GRCh38
NC_000008.10:g.129075934G= , CM000670.1:g.129075934G= GRCh37
NC_000008.9:g.129145116G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6472G=