Canonical Allele Identifier: CA15963304
Gene:
MyVariant.info:
GRCh38 chr20:g.6786464A>G
GRCh37 chr20:g.6767111A>G
gnomAD v2:
20:6767111 A / G
gnomAD v3:
20:6786464 A / G
gnomAD v4:
chr20-6786464-A-G
Joint Max Group AF 0.43538564 (AFR)
Genomes Max Group AF 0.43538564 (AFR)
ClinVar Allele:
983868
ClinVar RCV:
RCV001528157
ClinVar Variation:
996153
dbSNP:
235756
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.6786464A>G , CM000682.2:g.6786464A>G GRCh38
NC_000020.10:g.6767111A>G , CM000682.1:g.6767111A>G GRCh37
NC_000020.9:g.6715111A>G NCBI36
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