Canonical Allele Identifier: CA868687543
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1042045348
gnomAD v3: 9-94166936-A-AGGGCGGGAAGGCGC
gnomAD v4: 9-94166936-A-AGGGCGGGAAGGCGC
MyVariant Identifiers: chr9:g.96929218_96929219insGGGCGGGAAGGCGC (hg19) chr9:g.94166936_94166937insGGGCGGGAAGGCGC (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94166944_94166957dup , CM000671.2:g.94166944_94166957dup GRCh38
NC_000009.11:g.96929226_96929239dup , CM000671.1:g.96929226_96929239dup GRCh37
NC_000009.10:g.95969047_95969060dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+563_124+576dup
NR_170275.1:n.124+563_124+576dup
NR_170276.1:n.124+563_124+576dup
NR_170277.1:n.124+563_124+576dup
NR_170278.1:n.124+563_124+576dup
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