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Canonical Allele Identifier:
CA511291296
Gene: MIR646HG
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr20:g.58895827T>C (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.60320769T>C , CM000682.2:g.60320769T>C
GRCh38
NC_000020.10:g.58895827T>C , CM000682.1:g.58895827T>C
GRCh37
NC_000020.9:g.58329222T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_046099.1:n.556T>C
Search 100 bp 5'
Search 100 bp 3'