Canonical Allele Identifier: CA868687760

Gene: MIRLET7A1HG

Linked Data

• dbSNP Id: rs1268307320
• gnomAD v2: 9-96929646-A-T
• gnomAD v3: 9-94167364-A-T
• gnomAD v4: 9-94167364-A-T
• MyVariant Identifiers: chr9:g.96929646A>T (hg19) ; chr9:g.94167364A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94167364A>T , CM000671.2:g.94167364A>T	GRCh38
NC_000009.11:g.96929646A>T , CM000671.1:g.96929646A>T	GRCh37
NC_000009.10:g.95969467A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_170274.1:n.124+983A>T
NR_170275.1:n.124+983A>T
NR_170276.1:n.124+983A>T
NR_170277.1:n.124+983A>T
NR_170278.1:n.124+983A>T