Canonical Allele Identifier: CA1011013691
Gene: MIR181A1HG HGNC NCBI

Linked Data

dbSNP Id: rs969041101

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898171C>A , CM000663.2:g.198898171C>A GRCh38
NC_000001.10:g.198867300C>A , CM000663.1:g.198867300C>A GRCh37
NC_000001.9:g.197133923C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+2240G>T