ClinGen Allele Registry
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Canonical Allele Identifier:
CA511291278
Gene: MIR646HG
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr20:g.58895821T>G (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.60320763T>G , CM000682.2:g.60320763T>G
GRCh38
NC_000020.10:g.58895821T>G , CM000682.1:g.58895821T>G
GRCh37
NC_000020.9:g.58329216T>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_046099.1:n.550T>G
Search 100 bp 5'
Search 100 bp 3'