Canonical Allele Identifier: CA868687586
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1449900742
MyVariant Identifiers: chr9:g.96929273C>T (hg19) chr9:g.94166991C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94166991C>T , CM000671.2:g.94166991C>T GRCh38
NC_000009.11:g.96929273C>T , CM000671.1:g.96929273C>T GRCh37
NC_000009.10:g.95969094C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+610C>T
NR_170275.1:n.124+610C>T
NR_170276.1:n.124+610C>T
NR_170277.1:n.124+610C>T
NR_170278.1:n.124+610C>T
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