ClinGen Allele Registry
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Canonical Allele Identifier:
CA213050764
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.99591947A>G
GRCh37
chr10:g.101351704A>G
Linked Data - Sequence & Population
gnomAD v2:
10:101351704 A / G
gnomAD v3:
10:99591947 A / G
gnomAD v4:
chr10-99591947-A-G
Joint Max Group AF
0.26207949 (NFE)
Genomes Max Group AF
0.26207949 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11190164
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.99591947A>G , CM000672.2:g.99591947A>G
GRCh38
NC_000010.10:g.101351704A>G , CM000672.1:g.101351704A>G
GRCh37
NC_000010.9:g.101341694A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'