ClinGen Allele Registry
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Canonical Allele Identifier:
CA101676700
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.99353138A>G
GRCh37
chr4:g.100274295A>G
Linked Data - Sequence & Population
gnomAD v3:
4:99353138 A / G
gnomAD v4:
chr4-99353138-A-G
Joint Max Group AF
0.00005999 (SAS)
Genomes Max Group AF
0.00007293 (SAS)
Linked Data - NCBI & NCI
dbSNP:
559049461
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.99353138A>G , CM000666.2:g.99353138A>G
GRCh38
NC_000004.11:g.100274295A>G , CM000666.1:g.100274295A>G
GRCh37
NC_000004.10:g.100493318A>G
NCBI36
NG_011718.1:g.4623T>C
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