Canonical Allele Identifier: CA69802651
Gene:
MyVariant.info:
GRCh38 chr3:g.7870919G>A
GRCh37 chr3:g.7912606G>A
gnomAD v2:
3:7912606 G / A
gnomAD v3:
3:7870919 G / A
gnomAD v4:
chr3-7870919-G-A
Joint Max Group AF 0.14082873 (NFE)
Genomes Max Group AF 0.14082873 (NFE)
dbSNP:
7652838
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.7870919G>A , CM000665.2:g.7870919G>A GRCh38
NC_000003.11:g.7912606G>A , CM000665.1:g.7912606G>A GRCh37
NC_000003.10:g.7887606G>A NCBI36
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