Canonical Allele Identifier: CA11220560
Gene:
MyVariant.info:
GRCh38 chr2:g.5153392C>T
GRCh37 chr2:g.5293525C>T
gnomAD v2:
2:5293525 C / T
gnomAD v3:
2:5153392 C / T
gnomAD v4:
chr2-5153392-C-T
Joint Max Group AF 0.34875444 (EAS)
Genomes Max Group AF 0.34875444 (EAS)
dbSNP:
1377638
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.5153392C>T , CM000664.2:g.5153392C>T GRCh38
NC_000002.11:g.5293525C>T , CM000664.1:g.5293525C>T GRCh37
NC_000002.10:g.5210976C>T NCBI36
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