Canonical Allele Identifier: CA847233563

Gene: PVT1

Linked Data

• dbSNP Id: rs1466709920
• gnomAD v3: 8-128063561-C-G
• gnomAD v4: 8-128063561-C-G
• MyVariant Identifiers: chr8:g.129075807C>G (hg19) ; chr8:g.128063561C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128063561C>G , CM000670.2:g.128063561C>G	GRCh38
NC_000008.10:g.129075807C>G , CM000670.1:g.129075807C>G	GRCh37
NC_000008.9:g.129144989C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003367.3:n.1213-6599C>G