Canonical Allele Identifier: CA36189956

Gene: MIR181A1HG

Linked Data

• dbSNP Id: rs1023812126
• gnomAD v3: 1-198898341-T-C
• gnomAD v4: 1-198898341-T-C
• MyVariant Identifiers: chr1:g.198867470T>C (hg19) ; chr1:g.198898341T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198898341T>C , CM000663.2:g.198898341T>C	GRCh38
NC_000001.10:g.198867470T>C , CM000663.1:g.198867470T>C	GRCh37
NC_000001.9:g.197134093T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040073.1:n.363+2070A>G