Canonical Allele Identifier: CA1119063723
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1813859565
gnomAD v3: 8-128063570-AT-A
gnomAD v4: 8-128063570-AT-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063571del , CM000670.2:g.128063571del GRCh38
NC_000008.10:g.129075817del , CM000670.1:g.129075817del GRCh37
NC_000008.9:g.129144999del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6589del
Search 100 bp 5'
Search 100 bp 3'