Canonical Allele Identifier: CA589477072
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

gnomAD v2: 9-96929241-A-AGGGCGGGGGGGGGGG
gnomAD v3: 9-94166959-A-AGGGCGGGGGGGGGGG
gnomAD v4: 9-94166959-A-AGGGCGGGGGGGGGGG
MyVariant Identifiers: chr9:g.96929241_96929242insGGGCGGGGGGGGGGG (hg19) chr9:g.94166959_94166960insGGGCGGGGGGGGGGG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94166966_94166967insGGGGGGGGGGGCGGG , CM000671.2:g.94166966_94166967insGGGGGGGGGGGCGGG GRCh38
NC_000009.11:g.96929248_96929249insGGGGGGGGGGGCGGG , CM000671.1:g.96929248_96929249insGGGGGGGGGGGCGGG GRCh37
NC_000009.10:g.95969069_95969070insGGGGGGGGGGGCGGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+585_124+586insGGGGGGGGGGGCGGG
NR_170275.1:n.124+585_124+586insGGGGGGGGGGGCGGG
NR_170276.1:n.124+585_124+586insGGGGGGGGGGGCGGG
NR_170277.1:n.124+585_124+586insGGGGGGGGGGGCGGG
NR_170278.1:n.124+585_124+586insGGGGGGGGGGGCGGG
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