Canonical Allele Identifier: CA511291612

Gene: MIR646HG

Linked Data

• MyVariant Identifiers: chr20:g.58895937G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.60320879G>A , CM000682.2:g.60320879G>A	GRCh38
NC_000020.10:g.58895937G>A , CM000682.1:g.58895937G>A	GRCh37
NC_000020.9:g.58329332G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046099.1:n.666G>A