ClinGen Allele Registry
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Canonical Allele Identifier:
CA14939563
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.35379896A>G
GRCh37
chr22:g.35775889A>G
Linked Data - Sequence & Population
gnomAD v2:
22:35775889 A / G
gnomAD v3:
22:35379896 A / G
gnomAD v4:
chr22-35379896-A-G
Joint Max Group AF
0.83720365 (AFR)
Genomes Max Group AF
0.83720365 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3761439
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.35379896A>G , CM000684.2:g.35379896A>G
GRCh38
NC_000022.10:g.35775889A>G , CM000684.1:g.35775889A>G
GRCh37
NC_000022.9:g.34105889A>G
NCBI36
NG_023030.1:g.3830A>G
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