Canonical Allele Identifier: CA589477142

Gene: MIRLET7A1HG

Linked Data

• dbSNP Id: rs1052270272
• gnomAD v2: 9-96929672-C-G
• MyVariant Identifiers: chr9:g.96929672C>G (hg19) ; chr9:g.94167390C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94167390C>G , CM000671.2:g.94167390C>G	GRCh38
NC_000009.11:g.96929672C>G , CM000671.1:g.96929672C>G	GRCh37
NC_000009.10:g.95969493C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170274.1:n.124+1009C>G
NR_170275.1:n.124+1009C>G
NR_170276.1:n.124+1009C>G
NR_170277.1:n.124+1009C>G
NR_170278.1:n.124+1009C>G