Canonical Allele Identifier: CA196508983
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs370196159
gnomAD v2: 9-96929489-TCA-T
gnomAD v3: 9-94167207-TCA-T
gnomAD v4: 9-94167207-TCA-T
MyVariant Identifiers: chr9:g.96929490_96929491del (hg19) chr9:g.94167208_94167209del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94167208_94167209del , CM000671.2:g.94167208_94167209del GRCh38
NC_000009.11:g.96929490_96929491del , CM000671.1:g.96929490_96929491del GRCh37
NC_000009.10:g.95969311_95969312del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+827_124+828del
NR_170275.1:n.124+827_124+828del
NR_170276.1:n.124+827_124+828del
NR_170277.1:n.124+827_124+828del
NR_170278.1:n.124+827_124+828del
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