{{Rsnum
|rsid=121913388
|Chromosome=9
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CDKN2A
|position=21971121
|Gene_s=CDKN2A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600160
|rsnum=121913388
|variant=0002
}}{{ClinVar
|rsid=121913388
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=21971120
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=3
|VP=0x050268000000000002110120
|GENEINFO=CDKN2A:1029
|GENE_NAME=CDKN2A
|GENE_ID=1029
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.21971120G>A
|CLNORIGIN=2
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000010012.1; RCV000061923.2
|CLNDBN=Melanoma, cutaneous malignant, 2, susceptibility to; Malignant melanoma
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600160.0002
|Disease=Melanoma; Malignant melanoma
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0025202:2092003
}}{{PMID Auto
|PMID=21499247
|Title=Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
|OA=1
}}