ClinGen Allele Registry
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Canonical Allele Identifier:
CA511291303
Gene: MIR646HG
HGNC
NCBI
Linked Data
gnomAD v4:
20-60320772-A-G
MyVariant Identifiers:
chr20:g.58895830A>G (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.60320772A>G , CM000682.2:g.60320772A>G
GRCh38
NC_000020.10:g.58895830A>G , CM000682.1:g.58895830A>G
GRCh37
NC_000020.9:g.58329225A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_046099.1:n.559A>G
Search 100 bp 5'
Search 100 bp 3'