Canonical Allele Identifier: CA1119063747
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1813861162
gnomAD v3: 8-128063661-A-G
gnomAD v4: 8-128063661-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063661A>G , CM000670.2:g.128063661A>G GRCh38
NC_000008.10:g.129075907A>G , CM000670.1:g.129075907A>G GRCh37
NC_000008.9:g.129145089A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_003367.3:n.1213-6499A>G
Search 100 bp 5'
Search 100 bp 3'