Canonical Allele Identifier: CA185785078

Gene: PVT1

Linked Data

• dbSNP Id: rs568778442
• gnomAD v2: 8-128815066-T-C
• gnomAD v3: 8-127802820-T-C
• gnomAD v4: 8-127802820-T-C
• MyVariant Identifiers: chr8:g.128815066T>C (hg19) ; chr8:g.127802820T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127802820T>C , CM000670.2:g.127802820T>C	GRCh38
NC_000008.10:g.128815066T>C , CM000670.1:g.128815066T>C	GRCh37
NC_000008.9:g.128884248T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_003367.3:n.202+8086T>C