Canonical Allele Identifier: CA36189954

Gene: MIR181A1HG

Linked Data

• dbSNP Id: rs551451951
• gnomAD v2: 1-198867445-C-T
• gnomAD v3: 1-198898316-C-T
• gnomAD v4: 1-198898316-C-T
• MyVariant Identifiers: chr1:g.198867445C>T (hg19) ; chr1:g.198898316C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198898316C>T , CM000663.2:g.198898316C>T	GRCh38
NC_000001.10:g.198867445C>T , CM000663.1:g.198867445C>T	GRCh37
NC_000001.9:g.197134068C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040073.1:n.363+2095G>A