ClinGen Allele Registry
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Canonical Allele Identifier:
CA14800361
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.52967444A>G
GRCh37
chr20:g.51583983A>G
Linked Data - Sequence & Population
gnomAD v2:
20:51583983 A / G
gnomAD v3:
20:52967444 A / G
gnomAD v4:
chr20-52967444-A-G
Joint Max Group AF
0.1947849 (AMR)
Genomes Max Group AF
0.1947849 (AMR)
Linked Data - NCBI & NCI
dbSNP:
10485813
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.52967444A>G , CM000682.2:g.52967444A>G
GRCh38
NC_000020.10:g.51583983A>G , CM000682.1:g.51583983A>G
GRCh37
NC_000020.9:g.51017390A>G
NCBI36
NG_053184.1:g.136A>G
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