Canonical Allele Identifier: CA746165726

Gene: MIR646HG

Linked Data

• dbSNP Id: rs1481047098
• gnomAD v3: 20-60320788-GT-G
• gnomAD v4: 20-60320788-GT-G
• MyVariant Identifiers: chr20:g.58895847del (hg19) ; chr20:g.60320789del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.60320789del , CM000682.2:g.60320789del	GRCh38
NC_000020.10:g.58895847del , CM000682.1:g.58895847del	GRCh37
NC_000020.9:g.58329242del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046099.1:n.576del