Canonical Allele Identifier: CA511291579
Gene: MIR646HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.58895926A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320868A>G , CM000682.2:g.60320868A>G GRCh38
NC_000020.10:g.58895926A>G , CM000682.1:g.58895926A>G GRCh37
NC_000020.9:g.58329321A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.655A>G