ClinGen Allele Registry
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Canonical Allele Identifier:
CA14996872
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr22:g.33990484A>G
GRCh37
chr22:g.34386473A>G
Linked Data - Sequence & Population
gnomAD v2:
22:34386473 A / G
gnomAD v3:
22:33990484 A / G
gnomAD v4:
chr22-33990484-A-G
Joint Max Group AF
0.33113403 (AFR)
Genomes Max Group AF
0.33113403 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7286472
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.33990484A>G , CM000684.2:g.33990484A>G
GRCh38
NC_000022.10:g.34386473A>G , CM000684.1:g.34386473A>G
GRCh37
NC_000022.9:g.32716473A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'