ClinGen Allele Registry
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Canonical Allele Identifier:
CA13429180
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.113409552G>C
GRCh37
chr11:g.113280274G>C
Linked Data - Sequence & Population
gnomAD v2:
11:113280274 G / C
gnomAD v3:
11:113409552 G / C
gnomAD v4:
chr11-113409552-G-C
Joint Max Group AF
0.69362926 (NFE)
Genomes Max Group AF
0.69352451 (NFE)
Exomes Max Group AF
0.62939871 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2734842
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.113409552G>C , CM000673.2:g.113409552G>C
GRCh38
NC_000011.9:g.113280274G>C , CM000673.1:g.113280274G>C
GRCh37
NC_000011.8:g.112785484G>C
NCBI36
NG_008841.1:g.70728C>G
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