Canonical Allele Identifier: CA2653579489
Gene: MIR646HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320586T>C , CM000682.2:g.60320586T>C GRCh38
NC_000020.10:g.58895644T>C , CM000682.1:g.58895644T>C GRCh37
NC_000020.9:g.58329039T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.420-47T>C