Canonical Allele Identifier: CA41486736
Gene:
MyVariant.info:
GRCh38 chr2:g.632922G>A
GRCh37 chr2:g.632922G>A
gnomAD v2:
2:632922 G / A
gnomAD v3:
2:632922 G / A
gnomAD v4:
chr2-632922-G-A
Joint Max Group AF 0.89664772 (EAS)
Genomes Max Group AF 0.89664772 (EAS)
dbSNP:
62105303
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.632922G>A , CM000664.2:g.632922G>A GRCh38
NC_000002.11:g.632922G>A , CM000664.1:g.632922G>A GRCh37
NC_000002.10:g.622922G>A NCBI36
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