Canonical Allele Identifier: CA1126886094
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1828802098
gnomAD v3: 9-94167542-T-G
gnomAD v4: 9-94167542-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94167542T>G , CM000671.2:g.94167542T>G GRCh38
NC_000009.11:g.96929824T>G , CM000671.1:g.96929824T>G GRCh37
NC_000009.10:g.95969645T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+1161T>G
NR_170275.1:n.124+1161T>G
NR_170276.1:n.124+1161T>G
NR_170277.1:n.124+1161T>G
NR_170278.1:n.124+1161T>G