Canonical Allele Identifier: CA2373187802
Gene: MIR646HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.60320839C= , CM000682.2:g.60320839C= GRCh38
NC_000020.10:g.58895897C= , CM000682.1:g.58895897C= GRCh37
NC_000020.9:g.58329292C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046099.1:n.626C=