Canonical Allele Identifier: CA19503386
Gene:
MyVariant.info:
GRCh38 chr1:g.22376365G>A
GRCh37 chr1:g.22702858G>A
gnomAD v3:
1:22376365 G / A
gnomAD v4:
chr1-22376365-G-A
Joint Max Group AF 0.00007293 (SAS)
Genomes Max Group AF 0.00007293 (SAS)
dbSNP:
6696981
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22376365G>A , CM000663.2:g.22376365G>A GRCh38
NC_000001.10:g.22702858G>A , CM000663.1:g.22702858G>A GRCh37
NC_000001.9:g.22575445G>A NCBI36
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