ClinGen Allele Registry
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Canonical Allele Identifier:
CA773986509
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.63474767C>A
GRCh37
chr17:g.61552128C>A
Linked Data - Sequence & Population
gnomAD v3:
17:63474767 C / A
gnomAD v4:
chr17-63474767-C-A
Joint Max Group AF
0.00026249 (EAS)
Genomes Max Group AF
0.00026249 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4290
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.63474767C>A , CM000679.2:g.63474767C>A
GRCh38
NC_000017.10:g.61552128C>A , CM000679.1:g.61552128C>A
GRCh37
NC_000017.9:g.58905860C>A
NCBI36
NG_011648.1:g.2695C>A
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