Canonical Allele Identifier: CA589477103

Gene: MIRLET7A1HG

Linked Data

• dbSNP Id: rs1270063018
• gnomAD v2: 9-96929454-A-C
• gnomAD v3: 9-94167172-A-C
• gnomAD v4: 9-94167172-A-C
• MyVariant Identifiers: chr9:g.96929454A>C (hg19) ; chr9:g.94167172A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94167172A>C , CM000671.2:g.94167172A>C	GRCh38
NC_000009.11:g.96929454A>C , CM000671.1:g.96929454A>C	GRCh37
NC_000009.10:g.95969275A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170274.1:n.124+791A>C
NR_170275.1:n.124+791A>C
NR_170276.1:n.124+791A>C
NR_170277.1:n.124+791A>C
NR_170278.1:n.124+791A>C