ClinGen Allele Registry
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Canonical Allele Identifier:
CA16585050
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.51943113T>C
GRCh37
chr20:g.50559652T>C
Linked Data - Sequence & Population
gnomAD v2:
20:50559652 T / C
gnomAD v3:
20:51943113 T / C
gnomAD v4:
chr20-51943113-T-C
Joint Max Group AF
0.65429144 (AMR)
Genomes Max Group AF
0.65429144 (AMR)
Linked Data - NCBI & NCI
dbSNP:
6068020
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.51943113T>C , CM000682.2:g.51943113T>C
GRCh38
NC_000020.10:g.50559652T>C , CM000682.1:g.50559652T>C
GRCh37
NC_000020.9:g.49993059T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'