Canonical Allele Identifier: CA16217300
Gene:
MyVariant.info:
GRCh38 chr5:g.3939362G>A
GRCh37 chr5:g.3939476G>A
gnomAD v2:
5:3939476 G / A
gnomAD v3:
5:3939362 G / A
gnomAD v4:
chr5-3939362-G-A
Joint Max Group AF 0.59207056 (AFR)
Genomes Max Group AF 0.59207056 (AFR)
dbSNP:
492478
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.3939362G>A , CM000667.2:g.3939362G>A GRCh38
NC_000005.9:g.3939476G>A , CM000667.1:g.3939476G>A GRCh37
NC_000005.8:g.3992476G>A NCBI36
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