ClinGen Allele Registry
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Canonical Allele Identifier:
CA14926059
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr22:g.36216212C>G
GRCh37
chr22:g.36612258C>G
Linked Data - Sequence & Population
gnomAD v2:
22:36612258 C / G
gnomAD v3:
22:36216212 C / G
gnomAD v4:
chr22-36216212-C-G
Joint Max Group AF
0.32939531 (NFE)
Genomes Max Group AF
0.32939531 (NFE)
Linked Data - NCBI & NCI
dbSNP:
6000200
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.36216212C>G , CM000684.2:g.36216212C>G
GRCh38
NC_000022.10:g.36612258C>G , CM000684.1:g.36612258C>G
GRCh37
NC_000022.9:g.34942204C>G
NCBI36
Search 100 bp 5'
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