Canonical Allele Identifier: CA1818529766

Gene: PVT1

Linked Data

• dbSNP Id: rs1814479161

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127802713G>A , CM000670.2:g.127802713G>A	GRCh38
NC_000008.10:g.128814959G>A , CM000670.1:g.128814959G>A	GRCh37
NC_000008.9:g.128884141G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003367.3:n.202+7979G>A