Canonical Allele Identifier: CA209288658
Gene:
MyVariant.info:
GRCh38 chr10:g.69692529T>C
GRCh37 chr10:g.71452285T>C
gnomAD v2:
10:71452285 T / C
gnomAD v3:
10:69692529 T / C
gnomAD v4:
chr10-69692529-T-C
Joint Max Group AF 0.90825176 (EAS)
Genomes Max Group AF 0.90825176 (EAS)
Exomes Max Group AF 0.71979429 (NFE)
dbSNP:
2812533
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69692529T>C , CM000672.2:g.69692529T>C GRCh38
NC_000010.10:g.71452285T>C , CM000672.1:g.71452285T>C GRCh37
NC_000010.9:g.71122291T>C NCBI36
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