Canonical Allele Identifier: CA511291385
Gene: MIR646HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.58895859A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320801A>C , CM000682.2:g.60320801A>C GRCh38
NC_000020.10:g.58895859A>C , CM000682.1:g.58895859A>C GRCh37
NC_000020.9:g.58329254A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.588A>C