Canonical Allele Identifier: CA729928953

Gene: MIR181A1HG

Linked Data

• dbSNP Id: rs1385121004
• gnomAD v3: 1-198898287-T-C
• gnomAD v4: 1-198898287-T-C
• MyVariant Identifiers: chr1:g.198867416T>C (hg19) ; chr1:g.198898287T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198898287T>C , CM000663.2:g.198898287T>C	GRCh38
NC_000001.10:g.198867416T>C , CM000663.1:g.198867416T>C	GRCh37
NC_000001.9:g.197134039T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040073.1:n.363+2124A>G