ClinGen Allele Registry
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Canonical Allele Identifier:
CA14997041
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.36220399T>C
GRCh37
chr22:g.36616445T>C
Linked Data - Sequence & Population
gnomAD v2:
22:36616445 T / C
gnomAD v3:
22:36220399 T / C
gnomAD v4:
chr22-36220399-T-C
Joint Max Group AF
0.51809158 (AFR)
Genomes Max Group AF
0.51809158 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4821469
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.36220399T>C , CM000684.2:g.36220399T>C
GRCh38
NC_000022.10:g.36616445T>C , CM000684.1:g.36616445T>C
GRCh37
NC_000022.9:g.34946391T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'