ClinGen Allele Registry
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Canonical Allele Identifier:
CA13394651
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.102109604C>A
GRCh37
chr11:g.101980335C>A
Linked Data - Sequence & Population
gnomAD v2:
11:101980335 C / A
gnomAD v3:
11:102109604 C / A
gnomAD v4:
chr11-102109604-C-A
Joint Max Group AF
0.72079336 (EAS)
Genomes Max Group AF
0.72079336 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1820453
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.102109604C>A , CM000673.2:g.102109604C>A
GRCh38
NC_000011.9:g.101980335C>A , CM000673.1:g.101980335C>A
GRCh37
NC_000011.8:g.101485545C>A
NCBI36
NG_029530.1:g.4144C>A
NG_029530.2:g.4144C>A
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