Canonical Allele Identifier: CA1011013733
Gene: MIR181A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1658079515

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898393A>C , CM000663.2:g.198898393A>C GRCh38
NC_000001.10:g.198867522A>C , CM000663.1:g.198867522A>C GRCh37
NC_000001.9:g.197134145A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+2018T>G