Canonical Allele Identifier: CA589477064

Gene: MIRLET7A1HG

Linked Data

• dbSNP Id: rs1437333355
• gnomAD v2: 9-96929216-ACAGGGCGGGAAGGCGCGGGC-A
• gnomAD v3: 9-94166934-ACAGGGCGGGAAGGCGCGGGC-A
• gnomAD v4: 9-94166934-ACAGGGCGGGAAGGCGCGGGC-A
• MyVariant Identifiers: chr9:g.96929217_96929236del (hg19) ; chr9:g.94166935_94166954del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94166935_94166954del , CM000671.2:g.94166935_94166954del	GRCh38
NC_000009.11:g.96929217_96929236del , CM000671.1:g.96929217_96929236del	GRCh37
NC_000009.10:g.95969038_95969057del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170274.1:n.124+554_124+573del
NR_170275.1:n.124+554_124+573del
NR_170276.1:n.124+554_124+573del
NR_170277.1:n.124+554_124+573del
NR_170278.1:n.124+554_124+573del