ClinGen Allele Registry
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Canonical Allele Identifier:
CA13252993
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr10:g.117658593G>A
GRCh37
chr10:g.119418104G>A
Linked Data - Sequence & Population
gnomAD v2:
10:119418104 G / A
gnomAD v3:
10:117658593 G / A
gnomAD v4:
chr10-117658593-G-A
Joint Max Group AF
0.3920768 (NFE)
Genomes Max Group AF
0.3920768 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2184898
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.117658593G>A , CM000672.2:g.117658593G>A
GRCh38
NC_000010.10:g.119418104G>A , CM000672.1:g.119418104G>A
GRCh37
NC_000010.9:g.119408094G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'