Canonical Allele Identifier: CA15556990

Gene: PVT1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128046110G>A , CM000670.2:g.128046110G>A	GRCh38
NC_000008.10:g.129058356G>A , CM000670.1:g.129058356G>A	GRCh37
NC_000008.9:g.129127538G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003367.3:n.1213-24050G>A