Canonical Allele Identifier: CA4875562
Gene: PVT1 HGNC NCBI
MIR1206 HGNC NCBI
MyVariant.info:
GRCh38 chr8:g.128008933G>A
GRCh37 chr8:g.129021179G>A
gnomAD v2:
8:129021179 G / A
gnomAD v3:
8:128008933 G / A
gnomAD v4:
chr8-128008933-G-A
Joint Max Group AF 0.721681 (AFR)
Genomes Max Group AF 0.72171053 (AFR)
Exomes Max Group AF 0.71113789 (AFR)
dbSNP:
2114358
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128008933G>A , CM000670.2:g.128008933G>A GRCh38
NC_000008.10:g.129021179G>A , CM000670.1:g.129021179G>A GRCh37
NC_000008.9:g.129090361G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1212+19642G>A (PVT1)
NR_031611.1:n.36G>A (MIR1206)
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