Canonical Allele Identifier: CA15400299
Gene:
MyVariant.info:
GRCh38 chr5:g.4488132C>T
GRCh37 chr5:g.4488245C>T
gnomAD v2:
5:4488245 C / T
gnomAD v3:
5:4488132 C / T
gnomAD v4:
chr5-4488132-C-T
Joint Max Group AF 0.94745667 (EAS)
Genomes Max Group AF 0.94745667 (EAS)
dbSNP:
10462794
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.4488132C>T , CM000667.2:g.4488132C>T GRCh38
NC_000005.9:g.4488245C>T , CM000667.1:g.4488245C>T GRCh37
NC_000005.8:g.4541245C>T NCBI36
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