Canonical Allele Identifier: CA11143449
Gene:
MyVariant.info:
GRCh38 chr2:g.658595T>G
GRCh37 chr2:g.658595T>G
gnomAD v2:
2:658595 T / G
gnomAD v3:
2:658595 T / G
gnomAD v4:
chr2-658595-T-G
Joint Max Group AF 0.53473779 (EAS)
Genomes Max Group AF 0.53473779 (EAS)
dbSNP:
7596758
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.658595T>G , CM000664.2:g.658595T>G GRCh38
NC_000002.11:g.658595T>G , CM000664.1:g.658595T>G GRCh37
NC_000002.10:g.648595T>G NCBI36
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