Canonical Allele Identifier: CA14803039
Gene:
MyVariant.info:
GRCh38 chr20:g.187379T>C
GRCh37 chr20:g.168020T>C
gnomAD v2:
20:168020 T / C
gnomAD v3:
20:187379 T / C
gnomAD v4:
chr20-187379-T-C
Joint Max Group AF 0.28097653 (AFR)
Genomes Max Group AF 0.28097653 (AFR)
dbSNP:
13036722
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.187379T>C , CM000682.2:g.187379T>C GRCh38
NC_000020.10:g.168020T>C , CM000682.1:g.168020T>C GRCh37
NC_000020.9:g.116020T>C NCBI36
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