Canonical Allele Identifier: CA196508930
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs999308796
MyVariant Identifiers: chr9:g.96929370C>T (hg19) chr9:g.94167088C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94167088C>T , CM000671.2:g.94167088C>T GRCh38
NC_000009.11:g.96929370C>T , CM000671.1:g.96929370C>T GRCh37
NC_000009.10:g.95969191C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+707C>T
NR_170275.1:n.124+707C>T
NR_170276.1:n.124+707C>T
NR_170277.1:n.124+707C>T
NR_170278.1:n.124+707C>T
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