ClinGen Allele Registry
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Canonical Allele Identifier:
CA14934125
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.19168604T>C
GRCh37
chr22:g.19156117T>C
Linked Data - Sequence & Population
gnomAD v2:
22:19156117 T / C
gnomAD v3:
22:19168604 T / C
gnomAD v4:
chr22-19168604-T-C
Joint Max Group AF
0.78612735 (AFR)
Genomes Max Group AF
0.78612735 (AFR)
Linked Data - NCBI & NCI
dbSNP:
712964
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.19168604T>C , CM000684.2:g.19168604T>C
GRCh38
NC_000022.10:g.19156117T>C , CM000684.1:g.19156117T>C
GRCh37
NC_000022.9:g.17536117T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'