Canonical Allele Identifier: CA36189958

Gene: MIR181A1HG

Linked Data

• dbSNP Id: rs146899874
• gnomAD v2: 1-198867511-T-A
• gnomAD v3: 1-198898382-T-A
• gnomAD v4: 1-198898382-T-A
• MyVariant Identifiers: chr1:g.198867511T>A (hg19) ; chr1:g.198898382T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198898382T>A , CM000663.2:g.198898382T>A	GRCh38
NC_000001.10:g.198867511T>A , CM000663.1:g.198867511T>A	GRCh37
NC_000001.9:g.197134134T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040073.1:n.363+2029A>T