Canonical Allele Identifier: CA868687718

Gene: MIRLET7A1HG

Linked Data

• dbSNP Id: rs1424825294
• gnomAD v3: 9-94167266-G-GT
• gnomAD v4: 9-94167266-G-GT
• MyVariant Identifiers: chr9:g.96929548_96929549insT (hg19) ; chr9:g.94167266_94167267insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94167267dup , CM000671.2:g.94167267dup	GRCh38
NC_000009.11:g.96929549dup , CM000671.1:g.96929549dup	GRCh37
NC_000009.10:g.95969370dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170274.1:n.124+886dup
NR_170275.1:n.124+886dup
NR_170276.1:n.124+886dup
NR_170277.1:n.124+886dup
NR_170278.1:n.124+886dup