ClinGen Allele Registry
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Canonical Allele Identifier:
CA13170588
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.117433642C>A
GRCh37
chr10:g.119193153C>A
Linked Data - Sequence & Population
gnomAD v2:
10:119193153 C / A
gnomAD v3:
10:117433642 C / A
gnomAD v4:
chr10-117433642-C-A
Joint Max Group AF
0.77209971 (SAS)
Genomes Max Group AF
0.77209971 (SAS)
Linked Data - NCBI & NCI
dbSNP:
758569
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.117433642C>A , CM000672.2:g.117433642C>A
GRCh38
NC_000010.10:g.119193153C>A , CM000672.1:g.119193153C>A
GRCh37
NC_000010.9:g.119183143C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'