ClinGen Allele Registry
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Canonical Allele Identifier:
CA294733396
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.78925807C>G
GRCh37
chr17:g.76921889C>G
Linked Data - Sequence & Population
gnomAD v2:
17:76921889 C / G
gnomAD v3:
17:78925807 C / G
gnomAD v4:
chr17-78925807-C-G
Joint Max Group AF
0.15950141 (EAS)
Genomes Max Group AF
0.15950141 (EAS)
Linked Data - NCBI & NCI
dbSNP:
8179090
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.78925807C>G , CM000679.2:g.78925807C>G
GRCh38
NC_000017.10:g.76921889C>G , CM000679.1:g.76921889C>G
GRCh37
NC_000017.9:g.74433484C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'