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Canonical Allele Identifier:
CA11788059
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr4:g.117171981T>C
GRCh37
chr4:g.118093137T>C
Linked Data - Sequence & Population
gnomAD v2:
4:118093137 T / C
gnomAD v3:
4:117171981 T / C
gnomAD v4:
chr4-117171981-T-C
Joint Max Group AF
0.52856997 (EAS)
Genomes Max Group AF
0.52856997 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10433903
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.117171981T>C , CM000666.2:g.117171981T>C
GRCh38
NC_000004.11:g.118093137T>C , CM000666.1:g.118093137T>C
GRCh37
NC_000004.10:g.118312585T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'