Canonical Allele Identifier: CA868687730

Gene: MIRLET7A1HG

Linked Data

• dbSNP Id: rs1194461948
• gnomAD v3: 9-94167282-T-TA
• gnomAD v4: 9-94167282-T-TA
• MyVariant Identifiers: chr9:g.96929564_96929565insA (hg19) ; chr9:g.94167282_94167283insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94167284dup , CM000671.2:g.94167284dup	GRCh38
NC_000009.11:g.96929566dup , CM000671.1:g.96929566dup	GRCh37
NC_000009.10:g.95969387dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170274.1:n.124+903dup
NR_170275.1:n.124+903dup
NR_170276.1:n.124+903dup
NR_170277.1:n.124+903dup
NR_170278.1:n.124+903dup