Canonical Allele Identifier: CA746165568

Gene: MIR646HG

Linked Data

• dbSNP Id: rs1242612838
• gnomAD v3: 20-60320561-TAAG-T
• gnomAD v4: 20-60320561-TAAG-T
• MyVariant Identifiers: chr20:g.58895620_58895622del (hg19) ; chr20:g.60320562_60320564del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.60320566_60320568del , CM000682.2:g.60320566_60320568del	GRCh38
NC_000020.10:g.58895624_58895626del , CM000682.1:g.58895624_58895626del	GRCh37
NC_000020.9:g.58329019_58329021del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046099.1:n.420-67_420-65del