Canonical Allele Identifier: CA585790519
Gene:
MyVariant.info:
GRCh38 chr9:g.6365585T>C
GRCh37 chr9:g.6365585T>C
gnomAD v2:
9:6365585 T / C
gnomAD v3:
9:6365585 T / C
gnomAD v4:
chr9-6365585-T-C
Joint Max Group AF 0.00001171 (NFE)
Genomes Max Group AF 0.00001171 (NFE)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6365585T>C , CM000671.2:g.6365585T>C GRCh38
NC_000009.11:g.6365585T>C , CM000671.1:g.6365585T>C GRCh37
NC_000009.10:g.6355585T>C NCBI36
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