Canonical Allele Identifier: CA1126886050
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1828798353
gnomAD v3: 9-94167431-T-C
gnomAD v4: 9-94167431-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94167431T>C , CM000671.2:g.94167431T>C GRCh38
NC_000009.11:g.96929713T>C , CM000671.1:g.96929713T>C GRCh37
NC_000009.10:g.95969534T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+1050T>C
NR_170275.1:n.124+1050T>C
NR_170276.1:n.124+1050T>C
NR_170277.1:n.124+1050T>C
NR_170278.1:n.124+1050T>C