ClinGen Allele Registry
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Canonical Allele Identifier:
CA14921967
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.23580796A>G
GRCh37
chr22:g.23922983A>G
Linked Data - Sequence & Population
gnomAD v2:
22:23922983 A / G
gnomAD v3:
22:23580796 A / G
gnomAD v4:
chr22-23580796-A-G
Joint Max Group AF
0.77517682 (EAS)
Genomes Max Group AF
0.77506511 (EAS)
Exomes Max Group AF
0.54123132 (EAS)
Linked Data - NCBI & NCI
dbSNP:
140174
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.23580796A>G , CM000684.2:g.23580796A>G
GRCh38
NC_000022.10:g.23922983A>G , CM000684.1:g.23922983A>G
GRCh37
NC_000022.9:g.22252983A>G
NCBI36
NG_009791.1:g.4513T>C , LRG_69:g.4513T>C
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