Canonical Allele Identifier: CA190913805
Gene:
MyVariant.info:
GRCh38 chr9:g.17899608C>A
GRCh37 chr9:g.17899606C>A
gnomAD v3:
9:17899608 C / A
gnomAD v4:
chr9-17899608-C-A
Joint Max Group AF 0.00001972 (NFE)
Genomes Max Group AF 0.00001972 (NFE)
dbSNP:
1977882
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.17899608C>A , CM000671.2:g.17899608C>A GRCh38
NC_000009.11:g.17899606C>A , CM000671.1:g.17899606C>A GRCh37
NC_000009.10:g.17889606C>A NCBI36
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