Canonical Allele Identifier: CA36189966

Gene: MIR181A1HG

Linked Data

• dbSNP Id: rs200363142
• gnomAD v2: 1-198867594-A-AT
• gnomAD v3: 1-198898465-A-AT
• gnomAD v4: 1-198898465-A-AT
• MyVariant Identifiers: chr1:g.198867595_198867596insT (hg19) ; chr1:g.198867594_198867595insT (hg19) ; chr1:g.198898466_198898467insT (hg38) ; chr1:g.198898465_198898466insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198898473dup , CM000663.2:g.198898473dup	GRCh38
NC_000001.10:g.198867602dup , CM000663.1:g.198867602dup	GRCh37
NC_000001.9:g.197134225dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040073.1:n.363+1945dup