ClinGen Allele Registry
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Canonical Allele Identifier:
CA774000089
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.63901188A>C
GRCh37
chr17:g.61978548A>C
Linked Data - Sequence & Population
gnomAD v3:
17:63901188 A / C
gnomAD v4:
chr17-63901188-A-C
Joint Max Group AF
0.00016941 (EAS)
Genomes Max Group AF
0.00016941 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2941551
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.63901188A>C , CM000679.2:g.63901188A>C
GRCh38
NC_000017.10:g.61978548A>C , CM000679.1:g.61978548A>C
GRCh37
NC_000017.9:g.59332280A>C
NCBI36
NG_028354.1:g.474T>G
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