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Canonical Allele Identifier:
CA13443450
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.65745636T>C
GRCh37
chr11:g.65513107T>C
Linked Data - Sequence & Population
gnomAD v2:
11:65513107 T / C
gnomAD v3:
11:65745636 T / C
gnomAD v4:
chr11-65745636-T-C
Joint Max Group AF
0.87925451 (NFE)
Genomes Max Group AF
0.8792343 (NFE)
Exomes Max Group AF
0.57701769 (NFE)
Linked Data - NCBI & NCI
dbSNP:
593982
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.65745636T>C , CM000673.2:g.65745636T>C
GRCh38
NC_000011.9:g.65513107T>C , CM000673.1:g.65513107T>C
GRCh37
NC_000011.8:g.65269683T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'