ClinGen Allele Registry
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Canonical Allele Identifier:
CA14902335
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.34279939A>T
GRCh37
chr21:g.35652239A>T
Linked Data - Sequence & Population
gnomAD v2:
21:35652239 A / T
gnomAD v3:
21:34279939 A / T
gnomAD v4:
chr21-34279939-A-T
Joint Max Group AF
0.19025309 (AFR)
Genomes Max Group AF
0.19025309 (AFR)
Linked Data - NCBI & NCI
dbSNP:
9978142
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.34279939A>T , CM000683.2:g.34279939A>T
GRCh38
NC_000021.8:g.35652239A>T , CM000683.1:g.35652239A>T
GRCh37
NC_000021.7:g.34574109A>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'