ClinGen Allele Registry
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Canonical Allele Identifier:
CA13840636
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.22654552C>A
GRCh37
chr13:g.23228691C>A
Linked Data - Sequence & Population
gnomAD v2:
13:23228691 C / A
gnomAD v3:
13:22654552 C / A
gnomAD v4:
chr13-22654552-C-A
Joint Max Group AF
0.5921794 (AFR)
Genomes Max Group AF
0.5921794 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1034200
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.22654552C>A , CM000675.2:g.22654552C>A
GRCh38
NC_000013.10:g.23228691C>A , CM000675.1:g.23228691C>A
GRCh37
NC_000013.9:g.22126691C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'