Canonical Allele Identifier: CA589477075
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1466012040
gnomAD v2: 9-96929268-T-A
gnomAD v3: 9-94166986-T-A
gnomAD v4: 9-94166986-T-A
MyVariant Identifiers: chr9:g.96929268T>A (hg19) chr9:g.94166986T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94166986T>A , CM000671.2:g.94166986T>A GRCh38
NC_000009.11:g.96929268T>A , CM000671.1:g.96929268T>A GRCh37
NC_000009.10:g.95969089T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+605T>A
NR_170275.1:n.124+605T>A
NR_170276.1:n.124+605T>A
NR_170277.1:n.124+605T>A
NR_170278.1:n.124+605T>A
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