ClinGen Allele Registry
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Canonical Allele Identifier:
CA16587880
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.13514758A>G
GRCh37
chr21:g.14887079A>G
Linked Data - Sequence & Population
gnomAD v2:
21:14887079 A / G
gnomAD v3:
21:13514758 A / G
gnomAD v4:
chr21-13514758-A-G
Joint Max Group AF
0.86050425 (EAS)
Genomes Max Group AF
0.86050425 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11088680
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.13514758A>G , CM000683.2:g.13514758A>G
GRCh38
NC_000021.8:g.14887079A>G , CM000683.1:g.14887079A>G
GRCh37
NC_000021.7:g.13808950A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'