ClinGen Allele Registry
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Canonical Allele Identifier:
CA14795562
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.17611655A>G
GRCh37
chr20:g.17592300A>G
Linked Data - Sequence & Population
gnomAD v2:
20:17592300 A / G
gnomAD v3:
20:17611655 A / G
gnomAD v4:
chr20-17611655-A-G
Joint Max Group AF
0.55607871 (EAS)
Genomes Max Group AF
0.55607871 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12480819
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.17611655A>G , CM000682.2:g.17611655A>G
GRCh38
NC_000020.10:g.17592300A>G , CM000682.1:g.17592300A>G
GRCh37
NC_000020.9:g.17540300A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'