Canonical Allele Identifier: CA44282489
Gene:
MyVariant.info:
GRCh38 chr2:g.25343038A>G
GRCh37 chr2:g.25565907A>G
gnomAD v2:
2:25565907 A / G
gnomAD v3:
2:25343038 A / G
gnomAD v4:
chr2-25343038-A-G
Joint Max Group AF 0.9428332 (AFR)
Genomes Max Group AF 0.9428332 (AFR)
ClinVar RCV:
RCV001521676
ClinVar Variation:
706983
dbSNP:
1550117
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25343038A>G , CM000664.2:g.25343038A>G GRCh38
NC_000002.11:g.25565907A>G , CM000664.1:g.25565907A>G GRCh37
NC_000002.10:g.25419411A>G NCBI36
NG_029465.2:g.4553T>C , LRG_459:g.4553T>C
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