Canonical Allele Identifier: CA868687774
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs556435610
MyVariant Identifiers: chr9:g.96929697A>G (hg19) chr9:g.94167415A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94167415A>G , CM000671.2:g.94167415A>G GRCh38
NC_000009.11:g.96929697A>G , CM000671.1:g.96929697A>G GRCh37
NC_000009.10:g.95969518A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+1034A>G
NR_170275.1:n.124+1034A>G
NR_170276.1:n.124+1034A>G
NR_170277.1:n.124+1034A>G
NR_170278.1:n.124+1034A>G
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