Canonical Allele Identifier: CA585097039

Gene: PVT1

Linked Data

• dbSNP Id: rs1419306026
• gnomAD v2: 8-129075932-G-T
• gnomAD v3: 8-128063686-G-T
• gnomAD v4: 8-128063686-G-T
• MyVariant Identifiers: chr8:g.129075932G>T (hg19) ; chr8:g.128063686G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128063686G>T , CM000670.2:g.128063686G>T	GRCh38
NC_000008.10:g.129075932G>T , CM000670.1:g.129075932G>T	GRCh37
NC_000008.9:g.129145114G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_003367.3:n.1213-6474G>T