ClinGen Allele Registry
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Canonical Allele Identifier:
CA257634100
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.22139542G>T
Linked Data - Sequence & Population
gnomAD v3:
14:22139542 G / T
gnomAD v4:
chr14-22139542-G-T
Joint Max Group AF
0.14129303 (AFR)
Genomes Max Group AF
0.14129303 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1474476
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.22139542G>T , CM000676.2:g.22139542G>T
GRCh38
Search 100 bp 5'
Search 100 bp 3'