Canonical Allele Identifier: CA14595494
Gene:
MyVariant.info:
GRCh38 chr18:g.49560562C>T
GRCh37 chr18:g.47086932C>T
gnomAD v2:
18:47086932 C / T
gnomAD v3:
18:49560562 C / T
gnomAD v4:
chr18-49560562-C-T
Joint Max Group AF 0.94879318 (AFR)
Genomes Max Group AF 0.94879318 (AFR)
Exomes Max Group AF 0.57701769 (NFE)
dbSNP:
9958947
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49560562C>T , CM000680.2:g.49560562C>T GRCh38
NC_000018.9:g.47086932C>T , CM000680.1:g.47086932C>T GRCh37
NC_000018.8:g.45340930C>T NCBI36
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