ClinGen Allele Registry
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Canonical Allele Identifier:
CA102679401
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.102225733A>G
GRCh37
chr4:g.103146890A>G
Linked Data - Sequence & Population
gnomAD v3:
4:102225733 A / G
gnomAD v4:
chr4-102225733-A-G
Joint Max Group AF
0.00008899 (AMR)
Genomes Max Group AF
0.00008899 (AMR)
Linked Data - NCBI & NCI
dbSNP:
35518360
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.102225733A>G , CM000666.2:g.102225733A>G
GRCh38
NC_000004.11:g.103146890A>G , CM000666.1:g.103146890A>G
GRCh37
NC_000004.10:g.103365913A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'