Canonical Allele Identifier: CA113506398
Gene:
MyVariant.info:
GRCh38 chr5:g.4199820C>A
GRCh37 chr5:g.4199933C>A
gnomAD v2:
5:4199933 C / A
gnomAD v3:
5:4199820 C / A
gnomAD v4:
chr5-4199820-C-A
Joint Max Group AF 0.00082419 (SAS)
Genomes Max Group AF 0.00082419 (SAS)
dbSNP:
10036225
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.4199820C>A , CM000667.2:g.4199820C>A GRCh38
NC_000005.9:g.4199933C>A , CM000667.1:g.4199933C>A GRCh37
NC_000005.8:g.4252933C>A NCBI36
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