Canonical Allele Identifier: CA1818529759

Gene: PVT1

Linked Data

• dbSNP Id: rs1814479086

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127802706G>A , CM000670.2:g.127802706G>A	GRCh38
NC_000008.10:g.128814952G>A , CM000670.1:g.128814952G>A	GRCh37
NC_000008.9:g.128884134G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003367.3:n.202+7972G>A