Canonical Allele Identifier: CA196509023
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1006292039
gnomAD v3: 9-94167292-C-T
gnomAD v4: 9-94167292-C-T
MyVariant Identifiers: chr9:g.96929574C>T (hg19) chr9:g.94167292C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94167292C>T , CM000671.2:g.94167292C>T GRCh38
NC_000009.11:g.96929574C>T , CM000671.1:g.96929574C>T GRCh37
NC_000009.10:g.95969395C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_170274.1:n.124+911C>T
NR_170275.1:n.124+911C>T
NR_170276.1:n.124+911C>T
NR_170277.1:n.124+911C>T
NR_170278.1:n.124+911C>T
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