Canonical Allele Identifier: CA2600212286
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs2118235928
gnomAD v3: 9-94166948-C-G
gnomAD v4: 9-94166948-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94166948C>G , CM000671.2:g.94166948C>G GRCh38
NC_000009.11:g.96929230C>G , CM000671.1:g.96929230C>G GRCh37
NC_000009.10:g.95969051C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+567C>G
NR_170275.1:n.124+567C>G
NR_170276.1:n.124+567C>G
NR_170277.1:n.124+567C>G
NR_170278.1:n.124+567C>G