Canonical Allele Identifier: CA847233579

Gene: PVT1

Linked Data

• dbSNP Id: rs1253865073
• MyVariant Identifiers: chr8:g.129075859A>G (hg19) ; chr8:g.128063613A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128063613A>G , CM000670.2:g.128063613A>G	GRCh38
NC_000008.10:g.129075859A>G , CM000670.1:g.129075859A>G	GRCh37
NC_000008.9:g.129145041A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_003367.3:n.1213-6547A>G