Canonical Allele Identifier: CA13199029
Gene:
MyVariant.info:
GRCh38 chr10:g.92451547C>T
GRCh37 chr10:g.94211304C>T
gnomAD v2:
10:94211304 C / T
gnomAD v3:
10:92451547 C / T
gnomAD v4:
chr10-92451547-C-T
Joint Max Group AF 0.89878063 (EAS)
Genomes Max Group AF 0.89923878 (EAS)
Exomes Max Group AF 0.6856033 (EAS)
dbSNP:
2251101
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92451547C>T , CM000672.2:g.92451547C>T GRCh38
NC_000010.10:g.94211304C>T , CM000672.1:g.94211304C>T GRCh37
NC_000010.9:g.94201284C>T NCBI36
NG_013012.1:g.127549G>A
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