Canonical Allele Identifier: CA511291553
Gene: MIR646HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.58895917G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320859G>A , CM000682.2:g.60320859G>A GRCh38
NC_000020.10:g.58895917G>A , CM000682.1:g.58895917G>A GRCh37
NC_000020.9:g.58329312G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.646G>A