Canonical Allele Identifier: CA847233571

Gene: PVT1

Linked Data

• dbSNP Id: rs1252711416
• gnomAD v3: 8-128063585-A-C
• gnomAD v4: 8-128063585-A-C
• MyVariant Identifiers: chr8:g.129075831A>C (hg19) ; chr8:g.128063585A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128063585A>C , CM000670.2:g.128063585A>C	GRCh38
NC_000008.10:g.129075831A>C , CM000670.1:g.129075831A>C	GRCh37
NC_000008.9:g.129145013A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003367.3:n.1213-6575A>C