ClinGen Allele Registry
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Canonical Allele Identifier:
CA14870306
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.33316948A>G
GRCh37
chr21:g.34689253A>G
Linked Data - Sequence & Population
gnomAD v2:
21:34689253 A / G
gnomAD v3:
21:33316948 A / G
gnomAD v4:
chr21-33316948-A-G
Joint Max Group AF
0.89993015 (AFR)
Genomes Max Group AF
0.89993015 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2834188
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.33316948A>G , CM000683.2:g.33316948A>G
GRCh38
NC_000021.8:g.34689253A>G , CM000683.1:g.34689253A>G
GRCh37
NC_000021.7:g.33611123A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'