ClinGen Allele Registry
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Canonical Allele Identifier:
CA13369113
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.641191C>A
GRCh37
chr11:g.641191C>A
Linked Data - Sequence & Population
gnomAD v2:
11:641191 C / A
gnomAD v3:
11:641191 C / A
gnomAD v4:
chr11-641191-C-A
Joint Max Group AF
0.71004876 (EAS)
Genomes Max Group AF
0.71004876 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11246226
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.641191C>A , CM000673.2:g.641191C>A
GRCh38
NC_000011.9:g.641191C>A , CM000673.1:g.641191C>A
GRCh37
NC_000011.8:g.631191C>A
NCBI36
NG_021241.1:g.8887C>A
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