Canonical Allele Identifier: CA16046153
Gene:
MyVariant.info:
GRCh38 chr1:g.9091266C>T
GRCh37 chr1:g.9151325C>T
gnomAD v2:
1:9151325 C / T
gnomAD v3:
1:9091266 C / T
gnomAD v4:
chr1-9091266-C-T
Joint Max Group AF 0.20144713 (EAS)
Genomes Max Group AF 0.20144713 (EAS)
dbSNP:
12080794
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.9091266C>T , CM000663.2:g.9091266C>T GRCh38
NC_000001.10:g.9151325C>T , CM000663.1:g.9151325C>T GRCh37
NC_000001.9:g.9073912C>T NCBI36
NG_050918.1:g.7142G>A
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