Canonical Allele Identifier: CA586032959
Gene:
MyVariant.info:
GRCh38 chr9:g.1521204A>T
GRCh37 chr9:g.1521204A>T
gnomAD v2:
9:1521204 A / T
gnomAD v3:
9:1521204 A / T
gnomAD v4:
chr9-1521204-A-T
Joint Max Group AF 0.00000488 (NFE)
Genomes Max Group AF 0.00000488 (NFE)
dbSNP:
9886784
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1521204A>T , CM000671.2:g.1521204A>T GRCh38
NC_000009.11:g.1521204A>T , CM000671.1:g.1521204A>T GRCh37
NC_000009.10:g.1511204A>T NCBI36
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