Canonical Allele Identifier: CA422743711
Gene: MIR181A1HG HGNC NCBI

Linked Data

dbSNP Id: rs60639710
MyVariant Identifiers: chr1:g.198867678G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898549G>A , CM000663.2:g.198898549G>A GRCh38
NC_000001.10:g.198867678G>A , CM000663.1:g.198867678G>A GRCh37
NC_000001.9:g.197134301G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+1862C>T