ClinGen Allele Registry
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Canonical Allele Identifier:
CA11924291
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr5:g.29023197C>A
GRCh37
chr5:g.29023304C>A
Linked Data - Sequence & Population
gnomAD v2:
5:29023304 C / A
gnomAD v3:
5:29023197 C / A
gnomAD v4:
chr5-29023197-C-A
Joint Max Group AF
0.51243632 (EAS)
Genomes Max Group AF
0.51243632 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11750694
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.29023197C>A , CM000667.2:g.29023197C>A
GRCh38
NC_000005.9:g.29023304C>A , CM000667.1:g.29023304C>A
GRCh37
NC_000005.8:g.29059061C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'