ClinGen Allele Registry
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Canonical Allele Identifier:
CA13383072
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.57237593T>C
GRCh37
chr11:g.57005067T>C
Linked Data - Sequence & Population
gnomAD v2:
11:57005067 T / C
gnomAD v3:
11:57237593 T / C
gnomAD v4:
chr11-57237593-T-C
Joint Max Group AF
0.74819578 (EAS)
Genomes Max Group AF
0.74819578 (EAS)
Linked Data - NCBI & NCI
dbSNP:
9943582
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.57237593T>C , CM000673.2:g.57237593T>C
GRCh38
NC_000011.9:g.57005067T>C , CM000673.1:g.57005067T>C
GRCh37
NC_000011.8:g.56761643T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'