Canonical Allele Identifier: CA196509018
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs997366878
MyVariant Identifiers: chr9:g.96929563G>A (hg19) chr9:g.94167281G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94167281G>A , CM000671.2:g.94167281G>A GRCh38
NC_000009.11:g.96929563G>A , CM000671.1:g.96929563G>A GRCh37
NC_000009.10:g.95969384G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+900G>A
NR_170275.1:n.124+900G>A
NR_170276.1:n.124+900G>A
NR_170277.1:n.124+900G>A
NR_170278.1:n.124+900G>A
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