ClinGen Allele Registry
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Canonical Allele Identifier:
CA317000037
Gene: MIR646HG
HGNC
NCBI
Linked Data
dbSNP Id:
rs571764238
gnomAD v2:
20-58895614-G-C
gnomAD v3:
20-60320556-G-C
gnomAD v4:
20-60320556-G-C
MyVariant Identifiers:
chr20:g.58895614G>C (hg19)
chr20:g.60320556G>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.60320556G>C , CM000682.2:g.60320556G>C
GRCh38
NC_000020.10:g.58895614G>C , CM000682.1:g.58895614G>C
GRCh37
NC_000020.9:g.58329009G>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_046099.1:n.420-77G>C
Search 100 bp 5'
Search 100 bp 3'