ClinGen Allele Registry
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Canonical Allele Identifier:
CA13169731
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr10:g.113678445C>A
GRCh37
chr10:g.115438204C>A
Linked Data - Sequence & Population
gnomAD v2:
10:115438204 C / A
gnomAD v3:
10:113678445 C / A
gnomAD v4:
chr10-113678445-C-A
Joint Max Group AF
0.40651273 (EAS)
Genomes Max Group AF
0.40651273 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12415607
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.113678445C>A , CM000672.2:g.113678445C>A
GRCh38
NC_000010.10:g.115438204C>A , CM000672.1:g.115438204C>A
GRCh37
NC_000010.9:g.115428194C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'