Canonical Allele Identifier: CA185816184

Gene: PVT1

Linked Data

• dbSNP Id: rs527671418
• gnomAD v2: 8-129075664-A-G
• MyVariant Identifiers: chr8:g.129075664A>G (hg19) ; chr8:g.128063418A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128063418A>G , CM000670.2:g.128063418A>G	GRCh38
NC_000008.10:g.129075664A>G , CM000670.1:g.129075664A>G	GRCh37
NC_000008.9:g.129144846A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003367.3:n.1213-6742A>G