Canonical Allele Identifier: CA11219442
Gene:
MyVariant.info:
GRCh38 chr2:g.315215A>G
GRCh37 chr2:g.315215A>G
gnomAD v2:
2:315215 A / G
gnomAD v3:
2:315215 A / G
gnomAD v4:
chr2-315215-A-G
Joint Max Group AF 0.90956736 (NFE)
Genomes Max Group AF 0.90956736 (NFE)
dbSNP:
4643574
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.315215A>G , CM000664.2:g.315215A>G GRCh38
NC_000002.11:g.315215A>G , CM000664.1:g.315215A>G GRCh37
NC_000002.10:g.305215A>G NCBI36
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