Canonical Allele Identifier: CA185785063

Gene: PVT1

Linked Data

• dbSNP Id: rs920294707
• gnomAD v2: 8-128814995-C-G
• gnomAD v3: 8-127802749-C-G
• gnomAD v4: 8-127802749-C-G
• MyVariant Identifiers: chr8:g.128814995C>G (hg19) ; chr8:g.127802749C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127802749C>G , CM000670.2:g.127802749C>G	GRCh38
NC_000008.10:g.128814995C>G , CM000670.1:g.128814995C>G	GRCh37
NC_000008.9:g.128884177C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003367.3:n.202+8015C>G