Canonical Allele Identifier: CA511291624

Gene: MIR646HG

Linked Data

• dbSNP Id: rs1185957200
• gnomAD v3: 20-60320883-A-G
• gnomAD v4: 20-60320883-A-G
• MyVariant Identifiers: chr20:g.58895941A>G (hg19) ; chr20:g.60320883A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.60320883A>G , CM000682.2:g.60320883A>G	GRCh38
NC_000020.10:g.58895941A>G , CM000682.1:g.58895941A>G	GRCh37
NC_000020.9:g.58329336A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046099.1:n.670A>G