Canonical Allele Identifier: CA868687573
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1356835329
gnomAD v3: 9-94166969-A-G
gnomAD v4: 9-94166969-A-G
MyVariant Identifiers: chr9:g.96929251A>G (hg19) chr9:g.94166969A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94166969A>G , CM000671.2:g.94166969A>G GRCh38
NC_000009.11:g.96929251A>G , CM000671.1:g.96929251A>G GRCh37
NC_000009.10:g.95969072A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+588A>G
NR_170275.1:n.124+588A>G
NR_170276.1:n.124+588A>G
NR_170277.1:n.124+588A>G
NR_170278.1:n.124+588A>G
Search 100 bp 5'
Search 100 bp 3'