Canonical Allele Identifier: CA196508885
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs909469783
gnomAD v3: 9-94166989-C-G
gnomAD v4: 9-94166989-C-G
MyVariant Identifiers: chr9:g.94166989C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94166989C>G , CM000671.2:g.94166989C>G GRCh38
NC_000009.11:g.96929271C>G , CM000671.1:g.96929271C>G GRCh37
NC_000009.10:g.95969092C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+608C>G
NR_170275.1:n.124+608C>G
NR_170276.1:n.124+608C>G
NR_170277.1:n.124+608C>G
NR_170278.1:n.124+608C>G