Canonical Allele Identifier: CA11915332
Gene:
MyVariant.info:
GRCh38 chr5:g.583327G>A
GRCh37 chr5:g.583442G>A
gnomAD v2:
5:583442 G / A
gnomAD v3:
5:583327 G / A
gnomAD v4:
chr5-583327-G-A
Joint Max Group AF 0.20544322 (NFE)
Genomes Max Group AF 0.20544322 (NFE)
dbSNP:
4957048
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.583327G>A , CM000667.2:g.583327G>A GRCh38
NC_000005.9:g.583442G>A , CM000667.1:g.583442G>A GRCh37
NC_000005.8:g.636442G>A NCBI36
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