Canonical Allele Identifier: CA13120749
Gene:
MyVariant.info:
GRCh38 chr9:g.1521204A>C
GRCh37 chr9:g.1521204A>C
gnomAD v2:
9:1521204 A / C
gnomAD v3:
9:1521204 A / C
gnomAD v4:
chr9-1521204-A-C
Joint Max Group AF 0.80860287 (AMR)
Genomes Max Group AF 0.80860287 (AMR)
dbSNP:
9886784
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Genomic Alleles

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