Canonical Allele Identifier: CA1011013713
Gene: MIR181A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1658076508

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898263T>C , CM000663.2:g.198898263T>C GRCh38
NC_000001.10:g.198867392T>C , CM000663.1:g.198867392T>C GRCh37
NC_000001.9:g.197134015T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+2148A>G