Canonical Allele Identifier: CA511291322
Gene: MIR646HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.58895836A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320778A>C , CM000682.2:g.60320778A>C GRCh38
NC_000020.10:g.58895836A>C , CM000682.1:g.58895836A>C GRCh37
NC_000020.9:g.58329231A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.565A>C