Canonical Allele Identifier: CA12946259
Gene:
MyVariant.info:
GRCh38 chr9:g.1202371A>G
GRCh37 chr9:g.1202371A>G
gnomAD v2:
9:1202371 A / G
gnomAD v3:
9:1202371 A / G
gnomAD v4:
chr9-1202371-A-G
Joint Max Group AF 0.52275248 (EAS)
Genomes Max Group AF 0.52275248 (EAS)
dbSNP:
10809650
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1202371A>G , CM000671.2:g.1202371A>G GRCh38
NC_000009.11:g.1202371A>G , CM000671.1:g.1202371A>G GRCh37
NC_000009.10:g.1192371A>G NCBI36
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