Canonical Allele Identifier: CA216942487
Gene:
MyVariant.info:
GRCh38 chr11:g.636929C>T
GRCh37 chr11:g.636929C>T
gnomAD v2:
11:636929 C / T
gnomAD v3:
11:636929 C / T
gnomAD v4:
chr11-636929-C-T
Joint Max Group AF 0.15879139 (EAS)
Genomes Max Group AF 0.15879139 (EAS)
dbSNP:
916455
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.636929C>T , CM000673.2:g.636929C>T GRCh38
NC_000011.9:g.636929C>T , CM000673.1:g.636929C>T GRCh37
NC_000011.8:g.626929C>T NCBI36
NG_021241.1:g.4625C>T
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