Canonical Allele Identifier: CA196508965
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs962321075
MyVariant Identifiers: chr9:g.94167164G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94167164G>T , CM000671.2:g.94167164G>T GRCh38
NC_000009.11:g.96929446G>T , CM000671.1:g.96929446G>T GRCh37
NC_000009.10:g.95969267G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+783G>T
NR_170275.1:n.124+783G>T
NR_170276.1:n.124+783G>T
NR_170277.1:n.124+783G>T
NR_170278.1:n.124+783G>T