ClinGen Allele Registry
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Canonical Allele Identifier:
CA13166665
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.99781826A>G
GRCh37
chr10:g.101541583A>G
Linked Data - Sequence & Population
gnomAD v2:
10:101541583 A / G
gnomAD v3:
10:99781826 A / G
gnomAD v4:
chr10-99781826-A-G
Joint Max Group AF
0.43098436 (MID)
Genomes Max Group AF
0.42320998 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2804402
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.99781826A>G , CM000672.2:g.99781826A>G
GRCh38
NC_000010.10:g.101541583A>G , CM000672.1:g.101541583A>G
GRCh37
NC_000010.9:g.101531573A>G
NCBI36
NG_011798.1:g.4121A>G
NG_011798.2:g.4229A>G
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