Canonical Allele Identifier: CA13008945
Gene:
COSMIC:
COSN14868837 (not active)
MyVariant.info:
GRCh38 chr9:g.22125504G>C
GRCh37 chr9:g.22125503G>C
gnomAD v2:
9:22125503 G / C
gnomAD v3:
9:22125504 G / C
gnomAD v4:
chr9-22125504-G-C
Joint Max Group AF 0.4984772 (SAS)
Genomes Max Group AF 0.4984772 (SAS)
ClinVar RCV:
RCV001003460
ClinVar Variation:
812642
dbSNP:
1333049
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22125504G>C , CM000671.2:g.22125504G>C GRCh38
NC_000009.11:g.22125503G>C , CM000671.1:g.22125503G>C GRCh37
NC_000009.10:g.22115503G>C NCBI36
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