ClinGen Allele Registry
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Canonical Allele Identifier:
CA13179910
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr10:g.6064303T>C
GRCh37
chr10:g.6106266T>C
Linked Data - Sequence & Population
gnomAD v2:
10:6106266 T / C
gnomAD v3:
10:6064303 T / C
gnomAD v4:
chr10-6064303-T-C
Joint Max Group AF
0.54371504 (EAS)
Genomes Max Group AF
0.54371504 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7072793
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.6064303T>C , CM000672.2:g.6064303T>C
GRCh38
NC_000010.10:g.6106266T>C , CM000672.1:g.6106266T>C
GRCh37
NC_000010.9:g.6146272T>C
NCBI36
NG_007403.1:g.3007A>G , LRG_73:g.3007A>G
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