ClinGen Allele Registry
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Canonical Allele Identifier:
CA117710902
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr5:g.40424324A>G
Linked Data - Sequence & Population
gnomAD v3:
5:40424324 A / G
gnomAD v4:
chr5-40424324-A-G
Joint Max Group AF
0.00007276 (SAS)
Genomes Max Group AF
0.00007276 (SAS)
Linked Data - NCBI & NCI
dbSNP:
6896969
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.40424324A>G , CM000667.2:g.40424324A>G
GRCh38
NC_000005.9:g.40424426A>G , CM000667.1:g.40424426A>G
GRCh37
NC_000005.8:g.40460183A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'