Canonical Allele Identifier: CA422742915
Gene: MIR181A1HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.198867598T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898469T>C , CM000663.2:g.198898469T>C GRCh38
NC_000001.10:g.198867598T>C , CM000663.1:g.198867598T>C GRCh37
NC_000001.9:g.197134221T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+1942A>G