ClinGen Allele Registry
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Canonical Allele Identifier:
CA773985835
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.63473168C>G
GRCh37
chr17:g.61550529C>G
Linked Data - Sequence & Population
gnomAD v3:
17:63473168 C / G
gnomAD v4:
chr17-63473168-C-G
Linked Data - NCBI & NCI
dbSNP:
1800764
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.63473168C>G , CM000679.2:g.63473168C>G
GRCh38
NC_000017.10:g.61550529C>G , CM000679.1:g.61550529C>G
GRCh37
NC_000017.9:g.58904261C>G
NCBI36
NG_011648.1:g.1096C>G
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