Canonical Allele Identifier: CA13343403
Gene: CYP2C59P HGNC NCBI
MyVariant.info:
GRCh38 chr10:g.95007177A>C
GRCh37 chr10:g.96766934A>C
gnomAD v2:
10:96766934 A / C
gnomAD v3:
10:95007177 A / C
gnomAD v4:
chr10-95007177-A-C
Joint Max Group AF 0.78406632 (AFR)
Genomes Max Group AF 0.78323136 (AFR)
Exomes Max Group AF 0.77503404 (AFR)
dbSNP:
2860975
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95007177A>C , CM000672.2:g.95007177A>C GRCh38
NC_000010.10:g.96766934A>C , CM000672.1:g.96766934A>C GRCh37
NC_000010.9:g.96756924A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000457790.1:n.218T>G
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