ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA316729524
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.56248494A>G
GRCh37
chr20:g.54823550A>G
Linked Data - Sequence & Population
gnomAD v2:
20:54823550 A / G
gnomAD v3:
20:56248494 A / G
gnomAD v4:
chr20-56248494-A-G
Joint Max Group AF
0.11297109 (NFE)
Genomes Max Group AF
0.11297109 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11575886
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.56248494A>G , CM000682.2:g.56248494A>G
GRCh38
NC_000020.10:g.54823550A>G , CM000682.1:g.54823550A>G
GRCh37
NC_000020.9:g.54256957A>G
NCBI36
NG_012200.1:g.4763A>G
Search 100 bp 5'
Search 100 bp 3'