ClinGen Allele Registry
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Canonical Allele Identifier:
CA14859870
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.33362204C>A
GRCh37
chr21:g.34734510C>A
Linked Data - Sequence & Population
gnomAD v2:
21:34734510 C / A
gnomAD v3:
21:33362204 C / A
gnomAD v4:
chr21-33362204-C-A
Joint Max Group AF
0.36736417 (EAS)
Genomes Max Group AF
0.36736417 (EAS)
Linked Data - NCBI & NCI
dbSNP:
9980664
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.33362204C>A , CM000683.2:g.33362204C>A
GRCh38
NC_000021.8:g.34734510C>A , CM000683.1:g.34734510C>A
GRCh37
NC_000021.7:g.33656380C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'