Canonical Allele Identifier: CA185816186

Gene: PVT1

Linked Data

• dbSNP Id: rs936792604
• gnomAD v2: 8-129075683-G-A
• gnomAD v3: 8-128063437-G-A
• gnomAD v4: 8-128063437-G-A
• MyVariant Identifiers: chr8:g.129075683G>A (hg19) ; chr8:g.128063437G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128063437G>A , CM000670.2:g.128063437G>A	GRCh38
NC_000008.10:g.129075683G>A , CM000670.1:g.129075683G>A	GRCh37
NC_000008.9:g.129144865G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003367.3:n.1213-6723G>A