ClinGen Allele Registry
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Canonical Allele Identifier:
CA317000064
Gene: MIR646HG
HGNC
NCBI
Linked Data
dbSNP Id:
rs563675553
gnomAD v3:
20-60320812-A-T
gnomAD v4:
20-60320812-A-T
MyVariant Identifiers:
chr20:g.58895870A>T (hg19)
chr20:g.60320812A>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.60320812A>T , CM000682.2:g.60320812A>T
GRCh38
NC_000020.10:g.58895870A>T , CM000682.1:g.58895870A>T
GRCh37
NC_000020.9:g.58329265A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_046099.1:n.599A>T
Search 100 bp 5'
Search 100 bp 3'