ClinGen Allele Registry
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Canonical Allele Identifier:
CA15909011
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.63473168C>T
GRCh37
chr17:g.61550529C>T
Linked Data - Sequence & Population
gnomAD v2:
17:61550529 C / T
gnomAD v3:
17:63473168 C / T
gnomAD v4:
chr17-63473168-C-T
Joint Max Group AF
0.61679534 (EAS)
Genomes Max Group AF
0.61679534 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1800764
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.63473168C>T , CM000679.2:g.63473168C>T
GRCh38
NC_000017.10:g.61550529C>T , CM000679.1:g.61550529C>T
GRCh37
NC_000017.9:g.58904261C>T
NCBI36
NG_011648.1:g.1096C>T
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