Canonical Allele Identifier: CA422742948
Gene: MIR181A1HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.198867602T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898473T>G , CM000663.2:g.198898473T>G GRCh38
NC_000001.10:g.198867602T>G , CM000663.1:g.198867602T>G GRCh37
NC_000001.9:g.197134225T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+1938A>C