Canonical Allele Identifier: CA1865024879
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1050305641

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94167422G>C , CM000671.2:g.94167422G>C GRCh38
NC_000009.11:g.96929704G>C , CM000671.1:g.96929704G>C GRCh37
NC_000009.10:g.95969525G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_170274.1:n.124+1041G>C
NR_170275.1:n.124+1041G>C
NR_170276.1:n.124+1041G>C
NR_170277.1:n.124+1041G>C
NR_170278.1:n.124+1041G>C