Canonical Allele Identifier: CA847233602

Gene: PVT1

Linked Data

• dbSNP Id: rs1396949596
• gnomAD v3: 8-128063673-A-G
• gnomAD v4: 8-128063673-A-G
• MyVariant Identifiers: chr8:g.129075919A>G (hg19) ; chr8:g.128063673A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128063673A>G , CM000670.2:g.128063673A>G	GRCh38
NC_000008.10:g.129075919A>G , CM000670.1:g.129075919A>G	GRCh37
NC_000008.9:g.129145101A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_003367.3:n.1213-6487A>G