Canonical Allele Identifier: CA847202428

Gene: PVT1

Linked Data

• dbSNP Id: rs1182951267
• gnomAD v3: 8-127802702-G-A
• gnomAD v4: 8-127802702-G-A
• MyVariant Identifiers: chr8:g.128814948G>A (hg19) ; chr8:g.127802702G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127802702G>A , CM000670.2:g.127802702G>A	GRCh38
NC_000008.10:g.128814948G>A , CM000670.1:g.128814948G>A	GRCh37
NC_000008.9:g.128884130G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003367.3:n.202+7968G>A