Canonical Allele Identifier: CA13547578
Gene:
MyVariant.info:
GRCh38 chr11:g.269856C>T
GRCh37 chr11:g.269856C>T
gnomAD v2:
11:269856 C / T
gnomAD v3:
11:269856 C / T
gnomAD v4:
chr11-269856-C-T
Joint Max Group AF 0.25119646 (NFE)
Genomes Max Group AF 0.25119646 (NFE)
dbSNP:
7948797
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.269856C>T , CM000673.2:g.269856C>T GRCh38
NC_000011.9:g.269856C>T , CM000673.1:g.269856C>T GRCh37
NC_000011.8:g.259856C>T NCBI36
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