Canonical Allele Identifier: CA12948212
Gene:
MyVariant.info:
GRCh38 chr9:g.7682601C>A
GRCh37 chr9:g.7682601C>A
gnomAD v2:
9:7682601 C / A
gnomAD v3:
9:7682601 C / A
gnomAD v4:
chr9-7682601-C-A
Joint Max Group AF 0.60945526 (EAS)
Genomes Max Group AF 0.60945526 (EAS)
dbSNP:
842304
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.7682601C>A , CM000671.2:g.7682601C>A GRCh38
NC_000009.11:g.7682601C>A , CM000671.1:g.7682601C>A GRCh37
NC_000009.10:g.7672601C>A NCBI36
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