ClinGen Allele Registry
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Canonical Allele Identifier:
CA511291363
Gene: MIR646HG
HGNC
NCBI
Linked Data
dbSNP Id:
rs1240888270
gnomAD v2:
20-58895851-A-G
gnomAD v3:
20-60320793-A-G
gnomAD v4:
20-60320793-A-G
MyVariant Identifiers:
chr20:g.58895851A>G (hg19)
chr20:g.60320793A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.60320793A>G , CM000682.2:g.60320793A>G
GRCh38
NC_000020.10:g.58895851A>G , CM000682.1:g.58895851A>G
GRCh37
NC_000020.9:g.58329246A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_046099.1:n.580A>G
Search 100 bp 5'
Search 100 bp 3'