Canonical Allele Identifier: CA13092863
Gene:
MyVariant.info:
GRCh38 chr9:g.6166653G>A
GRCh37 chr9:g.6166653G>A
gnomAD v2:
9:6166653 G / A
gnomAD v3:
9:6166653 G / A
gnomAD v4:
chr9-6166653-G-A
Joint Max Group AF 0.341428 (NFE)
Genomes Max Group AF 0.341428 (NFE)
dbSNP:
2079
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6166653G>A , CM000671.2:g.6166653G>A GRCh38
NC_000009.11:g.6166653G>A , CM000671.1:g.6166653G>A GRCh37
NC_000009.10:g.6156653G>A NCBI36
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