Canonical Allele Identifier: CA847202442
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1260163258
MyVariant Identifiers: chr8:g.128814972G>A (hg19) chr8:g.127802726G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127802726G>A , CM000670.2:g.127802726G>A GRCh38
NC_000008.10:g.128814972G>A , CM000670.1:g.128814972G>A GRCh37
NC_000008.9:g.128884154G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.202+7992G>A
Search 100 bp 5'
Search 100 bp 3'