ClinGen Allele Registry
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Canonical Allele Identifier:
CA14917232
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.26171645A>G
GRCh37
chr21:g.27543963A>G
Linked Data - Sequence & Population
gnomAD v2:
21:27543963 A / G
gnomAD v3:
21:26171645 A / G
gnomAD v4:
chr21-26171645-A-G
Joint Max Group AF
0.19278198 (EAS)
Genomes Max Group AF
0.19278198 (EAS)
Linked Data - NCBI & NCI
dbSNP:
466433
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.26171645A>G , CM000683.2:g.26171645A>G
GRCh38
NC_000021.8:g.27543963A>G , CM000683.1:g.27543963A>G
GRCh37
NC_000021.7:g.26465834A>G
NCBI36
NG_007376.1:g.4170T>C
NG_007376.2:g.4484T>C
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