Canonical Allele Identifier: CA2513493530
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs2118236143

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94166966_94166967insT , CM000671.2:g.94166966_94166967insT GRCh38
NC_000009.11:g.96929248_96929249insT , CM000671.1:g.96929248_96929249insT GRCh37
NC_000009.10:g.95969069_95969070insT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+585_124+586insT
NR_170275.1:n.124+585_124+586insT
NR_170276.1:n.124+585_124+586insT
NR_170277.1:n.124+585_124+586insT
NR_170278.1:n.124+585_124+586insT