ClinGen Allele Registry
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Canonical Allele Identifier:
CA228201524
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.101178616T>C
GRCh37
chr11:g.101049347T>C
Linked Data - Sequence & Population
gnomAD v2:
11:101049347 T / C
gnomAD v3:
11:101178616 T / C
gnomAD v4:
chr11-101178616-T-C
Joint Max Group AF
0.86651331 (EAS)
Genomes Max Group AF
0.86651331 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1942836
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.101178616T>C , CM000673.2:g.101178616T>C
GRCh38
NC_000011.9:g.101049347T>C , CM000673.1:g.101049347T>C
GRCh37
NC_000011.8:g.100554557T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'