Canonical Allele Identifier: CA325105842

Gene: MIRLET7BHG

Linked Data

• dbSNP Id: rs35532365
• gnomAD v2: 22-46504357-G-GC
• gnomAD v3: 22-46108477-G-GC
• gnomAD v4: 22-46108477-G-GC
• MyVariant Identifiers: chr22:g.46504357_46504358insC (hg19) ; chr22:g.46108477_46108478insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46108478dup , CM000684.2:g.46108478dup	GRCh38
NC_000022.10:g.46504358dup , CM000684.1:g.46504358dup	GRCh37
NC_000022.9:g.44883022dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_027033.2:n.373-789dup
NR_110479.1:n.315-789dup