Canonical Allele Identifier: CA422742950
Gene: MIR181A1HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.198867603C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198898474C>G , CM000663.2:g.198898474C>G GRCh38
NC_000001.10:g.198867603C>G , CM000663.1:g.198867603C>G GRCh37
NC_000001.9:g.197134226C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040073.1:n.363+1937G>C