Canonical Allele Identifier: CA11843724
Gene:
MyVariant.info:
GRCh38 chr4:g.4717767A>G
GRCh37 chr4:g.4719494A>G
gnomAD v2:
4:4719494 A / G
gnomAD v3:
4:4717767 A / G
gnomAD v4:
chr4-4717767-A-G
Joint Max Group AF 0.55247751 (EAS)
Genomes Max Group AF 0.55247751 (EAS)
dbSNP:
1000579
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4717767A>G , CM000666.2:g.4717767A>G GRCh38
NC_000004.11:g.4719494A>G , CM000666.1:g.4719494A>G GRCh37
NC_000004.10:g.4770395A>G NCBI36
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