Canonical Allele Identifier: CA15552757

Gene: PVT1

Linked Data

• dbSNP Id: rs2608053
• gnomAD v2: 8-129075832-T-C
• gnomAD v3: 8-128063586-T-C
• gnomAD v4: 8-128063586-T-C
• MyVariant Identifiers: chr8:g.129075832T>C (hg19) ; chr8:g.128063586T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128063586T>C , CM000670.2:g.128063586T>C	GRCh38
NC_000008.10:g.129075832T>C , CM000670.1:g.129075832T>C	GRCh37
NC_000008.9:g.129145014T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_003367.3:n.1213-6574T>C