Canonical Allele Identifier: CA868687798

Gene: MIRLET7A1HG

Linked Data

• dbSNP Id: rs1334766945
• gnomAD v3: 9-94167522-C-A
• gnomAD v4: 9-94167522-C-A
• MyVariant Identifiers: chr9:g.96929804C>A (hg19) ; chr9:g.94167522C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94167522C>A , CM000671.2:g.94167522C>A	GRCh38
NC_000009.11:g.96929804C>A , CM000671.1:g.96929804C>A	GRCh37
NC_000009.10:g.95969625C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170274.1:n.124+1141C>A
NR_170275.1:n.124+1141C>A
NR_170276.1:n.124+1141C>A
NR_170277.1:n.124+1141C>A
NR_170278.1:n.124+1141C>A