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Canonical Allele Identifier:
CA124880749
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.111078033C>G
GRCh37
chr5:g.110413731C>G
Linked Data - Sequence & Population
gnomAD v2:
5:110413731 C / G
gnomAD v3:
5:111078033 C / G
gnomAD v4:
chr5-111078033-C-G
Joint Max Group AF
0.26568342 (SAS)
Genomes Max Group AF
0.26568342 (SAS)
Exomes Max Group AF
0.17768 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11466754
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.111078033C>G , CM000667.2:g.111078033C>G
GRCh38
NC_000005.9:g.110413731C>G , CM000667.1:g.110413731C>G
GRCh37
NC_000005.8:g.110441630C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'