ClinGen Allele Registry
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Canonical Allele Identifier:
CA14920212
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.19703979T>C
GRCh37
chr22:g.19691502T>C
Linked Data - Sequence & Population
gnomAD v2:
22:19691502 T / C
gnomAD v3:
22:19703979 T / C
gnomAD v4:
chr22-19703979-T-C
Joint Max Group AF
0.82402247 (AFR)
Genomes Max Group AF
0.82402247 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4819833
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.19703979T>C , CM000684.2:g.19703979T>C
GRCh38
NC_000022.10:g.19691502T>C , CM000684.1:g.19691502T>C
GRCh37
NC_000022.9:g.18071502T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'