Canonical Allele Identifier: CA196509040

Gene: MIRLET7A1HG

Linked Data

• dbSNP Id: rs34917169
• MyVariant Identifiers: chr9:g.96929600_96929601insG (hg19) ; chr9:g.94167318_94167319insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94167318_94167319insG , CM000671.2:g.94167318_94167319insG	GRCh38
NC_000009.11:g.96929600_96929601insG , CM000671.1:g.96929600_96929601insG	GRCh37
NC_000009.10:g.95969421_95969422insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170274.1:n.124+937_124+938insG
NR_170275.1:n.124+937_124+938insG
NR_170276.1:n.124+937_124+938insG
NR_170277.1:n.124+937_124+938insG
NR_170278.1:n.124+937_124+938insG