ClinGen Allele Registry
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Canonical Allele Identifier:
CA15976847
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.21899407A>G
GRCh37
chr20:g.21880045A>G
Linked Data - Sequence & Population
gnomAD v2:
20:21880045 A / G
gnomAD v3:
20:21899407 A / G
gnomAD v4:
chr20-21899407-A-G
Joint Max Group AF
0.78186053 (AFR)
Genomes Max Group AF
0.78186053 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1998076
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.21899407A>G , CM000682.2:g.21899407A>G
GRCh38
NC_000020.10:g.21880045A>G , CM000682.1:g.21880045A>G
GRCh37
NC_000020.9:g.21828045A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'