Canonical Allele Identifier: CA2373187759
Gene: MIR646HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320717C= , CM000682.2:g.60320717C= GRCh38
NC_000020.10:g.58895775C= , CM000682.1:g.58895775C= GRCh37
NC_000020.9:g.58329170C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.504C=