Canonical Allele Identifier: CA1126885741

Gene: MIRLET7A1HG

Linked Data

• dbSNP Id: rs2118236109
• gnomAD v3: 9-94166963-C-CGGGGGGGGGGGGGGG
• gnomAD v4: 9-94166963-C-CGGGGGGGGGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94166966_94166967insGGGGGGGGGGGGGGG , CM000671.2:g.94166966_94166967insGGGGGGGGGGGGGGG	GRCh38
NC_000009.11:g.96929248_96929249insGGGGGGGGGGGGGGG , CM000671.1:g.96929248_96929249insGGGGGGGGGGGGGGG	GRCh37
NC_000009.10:g.95969069_95969070insGGGGGGGGGGGGGGG	NCBI36

Transcript Alleles

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