Canonical Allele Identifier: CA1011013769
Gene: MIR181A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1658080288

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898453T>C , CM000663.2:g.198898453T>C GRCh38
NC_000001.10:g.198867582T>C , CM000663.1:g.198867582T>C GRCh37
NC_000001.9:g.197134205T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+1958A>G