Canonical Allele Identifier: CA1011013694
Gene: MIR181A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1658075625

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898190A>T , CM000663.2:g.198898190A>T GRCh38
NC_000001.10:g.198867319A>T , CM000663.1:g.198867319A>T GRCh37
NC_000001.9:g.197133942A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+2221T>A