Canonical Allele Identifier: CA196508872
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs975759681
gnomAD v2: 9-96929254-C-A
gnomAD v3: 9-94166972-C-A
gnomAD v4: 9-94166972-C-A
MyVariant Identifiers: chr9:g.96929254C>A (hg19) chr9:g.94166972C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94166972C>A , CM000671.2:g.94166972C>A GRCh38
NC_000009.11:g.96929254C>A , CM000671.1:g.96929254C>A GRCh37
NC_000009.10:g.95969075C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+591C>A
NR_170275.1:n.124+591C>A
NR_170276.1:n.124+591C>A
NR_170277.1:n.124+591C>A
NR_170278.1:n.124+591C>A
Search 100 bp 5'
Search 100 bp 3'