Canonical Allele Identifier: CA1865024999
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1334766945

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94167522C>T , CM000671.2:g.94167522C>T GRCh38
NC_000009.11:g.96929804C>T , CM000671.1:g.96929804C>T GRCh37
NC_000009.10:g.95969625C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+1141C>T
NR_170275.1:n.124+1141C>T
NR_170276.1:n.124+1141C>T
NR_170277.1:n.124+1141C>T
NR_170278.1:n.124+1141C>T