Canonical Allele Identifier: CA1126886105
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1828802903
gnomAD v3: 9-94167572-T-C
gnomAD v4: 9-94167572-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94167572T>C , CM000671.2:g.94167572T>C GRCh38
NC_000009.11:g.96929854T>C , CM000671.1:g.96929854T>C GRCh37
NC_000009.10:g.95969675T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+1191T>C
NR_170275.1:n.124+1191T>C
NR_170276.1:n.124+1191T>C
NR_170277.1:n.124+1191T>C
NR_170278.1:n.124+1191T>C