ClinGen Allele Registry
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Canonical Allele Identifier:
CA14948201
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.21454896T>C
GRCh37
chr22:g.21809185T>C
Linked Data - Sequence & Population
gnomAD v2:
22:21809185 T / C
gnomAD v3:
22:21454896 T / C
gnomAD v4:
chr22-21454896-T-C
Joint Max Group AF
0.7008076 (NFE)
Genomes Max Group AF
0.7008076 (NFE)
Linked Data - NCBI & NCI
dbSNP:
463426
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.21454896T>C , CM000684.2:g.21454896T>C
GRCh38
NC_000022.10:g.21809185T>C , CM000684.1:g.21809185T>C
GRCh37
NC_000022.9:g.20139185T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'