Canonical Allele Identifier: CA2600212342
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs2118239972
gnomAD v3: 9-94167549-T-A
gnomAD v4: 9-94167549-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94167549T>A , CM000671.2:g.94167549T>A GRCh38
NC_000009.11:g.96929831T>A , CM000671.1:g.96929831T>A GRCh37
NC_000009.10:g.95969652T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+1168T>A
NR_170275.1:n.124+1168T>A
NR_170276.1:n.124+1168T>A
NR_170277.1:n.124+1168T>A
NR_170278.1:n.124+1168T>A