Canonical Allele Identifier: CA14757899
Gene:
MyVariant.info:
GRCh38 chr20:g.44436388A>C
GRCh37 chr20:g.43065028A>C
gnomAD v2:
20:43065028 A / C
gnomAD v3:
20:44436388 A / C
gnomAD v4:
chr20-44436388-A-C
Joint Max Group AF 0.8713082 (EAS)
Genomes Max Group AF 0.87029134 (EAS)
Exomes Max Group AF 0.80980832 (EAS)
dbSNP:
6017342
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44436388A>C , CM000682.2:g.44436388A>C GRCh38
NC_000020.10:g.43065028A>C , CM000682.1:g.43065028A>C GRCh37
NC_000020.9:g.42498442A>C NCBI36
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