Canonical Allele Identifier: CA2816894349
Gene: MIR646HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320594C>A , CM000682.2:g.60320594C>A GRCh38
NC_000020.10:g.58895652C>A , CM000682.1:g.58895652C>A GRCh37
NC_000020.9:g.58329047C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.420-39C>A