ClinGen Allele Registry
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Canonical Allele Identifier:
CA15651569
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.67920067T>C
GRCh37
chr10:g.69679824T>C
Linked Data - Sequence & Population
gnomAD v2:
10:69679824 T / C
gnomAD v3:
10:67920067 T / C
gnomAD v4:
chr10-67920067-T-C
Joint Max Group AF
0.67308001 (NFE)
Genomes Max Group AF
0.67308001 (NFE)
Linked Data - NCBI & NCI
dbSNP:
10997875
2131441233
2131441245
2131441250
2131441264
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.67920067T>C , CM000672.2:g.67920067T>C
GRCh38
NC_000010.10:g.69679824T>C , CM000672.1:g.69679824T>C
GRCh37
NC_000010.9:g.69349830T>C
NCBI36
NG_050664.1:g.40406T>C
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