{
  "@context": "http://reg.genome.network/schema/allele.jsonld",
  "@id": "http://reg.genome.network/allele/CA013249",
  "communityStandardTitle": [
    "NM_000138.5(FBN1):c.2638G>A (p.Gly880Ser)"
  ],
  "externalRecords": {
    "ClinVarAlleles": [
      {
        "@id": "http://www.ncbi.nlm.nih.gov/clinvar/?term=197756[alleleid]",
        "alleleId": 197756,
        "preferredName": "NM_000138.5(FBN1):c.2638G>A (p.Gly880Ser)"
      }
    ],
    "ClinVarVariations": [
      {
        "@id": "http://www.ncbi.nlm.nih.gov/clinvar/variation/200000",
        "RCV": [
          "RCV000556229",
          "RCV000663561",
          "RCV000769644",
          "RCV001269745"
        ],
        "variationId": 200000
      }
    ],
    "MyVariantInfo_hg19": [
      {
        "@id": "http://myvariant.info/v1/variant/chr15:g.48787359C>T?assembly=hg19",
        "id": "chr15:g.48787359C>T"
      }
    ],
    "MyVariantInfo_hg38": [
      {
        "@id": "http://myvariant.info/v1/variant/chr15:g.48495162C>T?assembly=hg38",
        "id": "chr15:g.48495162C>T"
      }
    ],
    "dbSNP": [
      {
        "@id": "http://www.ncbi.nlm.nih.gov/snp/794728194",
        "rs": 794728194
      }
    ],
    "gnomAD_2": [
      {
        "@id": "http://gnomad.broadinstitute.org/variant/15-48787359-C-T?dataset=gnomad_r2_1",
        "id": "15-48787359-C-T",
        "variant": "15:48787359 C / T"
      }
    ],
    "gnomAD_4": [
      {
        "@id": "http://gnomad.broadinstitute.org/variant/15-48495162-C-T?dataset=gnomad_r4",
        "id": "15-48495162-C-T",
        "variant": "15:48495162 C / T"
      }
    ]
  },
  "genomicAlleles": [
    {
      "chromosome": "15",
      "coordinates": [
        {
          "allele": "T",
          "end": 48495162,
          "referenceAllele": "C",
          "start": 48495161
        }
      ],
      "hgvs": [
        "NC_000015.10:g.48495162C>T",
        "CM000677.2:g.48495162C>T"
      ],
      "referenceGenome": "GRCh38",
      "referenceSequence": "http://reg.genome.network/refseq/RS000063"
    },
    {
      "chromosome": "15",
      "coordinates": [
        {
          "allele": "T",
          "end": 48787359,
          "referenceAllele": "C",
          "start": 48787358
        }
      ],
      "hgvs": [
        "NC_000015.9:g.48787359C>T",
        "CM000677.1:g.48787359C>T"
      ],
      "referenceGenome": "GRCh37",
      "referenceSequence": "http://reg.genome.network/refseq/RS000039"
    },
    {
      "chromosome": "15",
      "coordinates": [
        {
          "allele": "T",
          "end": 46574651,
          "referenceAllele": "C",
          "start": 46574650
        }
      ],
      "hgvs": [
        "NC_000015.8:g.46574651C>T"
      ],
      "referenceGenome": "NCBI36",
      "referenceSequence": "http://reg.genome.network/refseq/RS000015"
    },
    {
      "coordinates": [
        {
          "allele": "A",
          "end": 155627,
          "referenceAllele": "G",
          "start": 155626
        }
      ],
      "hgvs": [
        "NG_008805.2:g.155627G>A",
        "LRG_778:g.155627G>A"
      ],
      "referenceSequence": "http://reg.genome.network/refseq/RS001224"
    }
  ],
  "transcriptAlleles": [
    {
      "coordinates": [
        {
          "allele": "A",
          "end": 2954,
          "referenceAllele": "G",
          "start": 2953
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003603",
      "geneNCBI_id": 2200,
      "geneSymbol": "FBN1",
      "hgvs": [
        "ENST00000559133.6:c.2638G>A"
      ],
      "proteinEffect": {
        "hgvs": "ENSP00000453958.2:p.Gly880Ser",
        "hgvsWellDefined": "ENSP00000453958.2:p.Gly880Ser"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS914274"
    },
    {
      "coordinates": [
        {
          "allele": "A",
          "end": 2954,
          "referenceAllele": "G",
          "start": 2953
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003603",
      "geneNCBI_id": 2200,
      "geneSymbol": "FBN1",
      "hgvs": [
        "ENST00000674301.2:c.2638G>A"
      ],
      "proteinEffect": {
        "hgvs": "ENSP00000501333.2:p.Gly880Ser",
        "hgvsWellDefined": "ENSP00000501333.2:p.Gly880Ser"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS914454"
    },
    {
      "coordinates": [
        {
          "allele": "A",
          "end": 1312,
          "referenceAllele": "G",
          "start": 1311
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003603",
      "geneNCBI_id": 2200,
      "geneSymbol": "FBN1",
      "hgvs": [
        "ENST00000684448.1:n.1312G>A"
      ],
      "referenceSequence": "http://reg.genome.network/refseq/RS829402"
    },
    {
      "coordinates": [
        {
          "allele": "A",
          "end": 2954,
          "referenceAllele": "G",
          "start": 2953
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003603",
      "geneNCBI_id": 2200,
      "geneSymbol": "FBN1",
      "hgvs": [
        "ENST00000316623.10:c.2638G>A"
      ],
      "proteinEffect": {
        "hgvs": "ENSP00000325527.5:p.Gly880Ser",
        "hgvsWellDefined": "ENSP00000325527.5:p.Gly880Ser"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS746076",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000316623.10:c.2638G>A"
          },
          "RefSeq": {
            "hgvs": "NM_000138.5:c.2638G>A"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000325527.5:p.Gly880Ser"
          },
          "RefSeq": {
            "hgvs": "NP_000129.3:p.Gly880Ser"
          }
        }
      }
    },
    {
      "coordinates": [
        {
          "allele": "A",
          "end": 3094,
          "referenceAllele": "G",
          "start": 3093
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003603",
      "geneNCBI_id": 2200,
      "geneSymbol": "FBN1",
      "hgvs": [
        "ENST00000316623.9:c.2638G>A"
      ],
      "proteinEffect": {
        "hgvs": "ENSP00000325527.5:p.Gly880Ser",
        "hgvsWellDefined": "ENSP00000325527.5:p.Gly880Ser"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS247158"
    },
    {
      "coordinates": [
        {
          "allele": "A",
          "end": 952,
          "endIntronDirection": "-",
          "endIntronOffset": 20511,
          "referenceAllele": "G",
          "start": 952,
          "startIntronDirection": "-",
          "startIntronOffset": 20512
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003603",
      "geneNCBI_id": 2200,
      "geneSymbol": "FBN1",
      "hgvs": [
        "ENST00000537463.6:c.637-20512G>A"
      ],
      "proteinEffect": {
        "hgvs": "ENSP00000440294.2:n.637-20512G>A"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS360786"
    },
    {
      "@id": "http://reg.genome.network/allele/PA304072",
      "coordinates": [
        {
          "allele": "A",
          "end": 3033,
          "referenceAllele": "G",
          "start": 3032
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003603",
      "geneNCBI_id": 2200,
      "geneSymbol": "FBN1",
      "hgvs": [
        "NM_000138.4:c.2638G>A",
        "LRG_778t1:c.2638G>A"
      ],
      "proteinEffect": {
        "hgvs": "NP_000129.3:p.Gly880Ser",
        "hgvsWellDefined": "NP_000129.3:p.Gly880Ser"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS006200"
    },
    {
      "@id": "http://reg.genome.network/allele/PA304072",
      "coordinates": [
        {
          "allele": "A",
          "end": 2954,
          "referenceAllele": "G",
          "start": 2953
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003603",
      "geneNCBI_id": 2200,
      "geneSymbol": "FBN1",
      "hgvs": [
        "NM_000138.5:c.2638G>A"
      ],
      "proteinEffect": {
        "hgvs": "NP_000129.3:p.Gly880Ser",
        "hgvsWellDefined": "NP_000129.3:p.Gly880Ser"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS674722",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000316623.10:c.2638G>A"
          },
          "RefSeq": {
            "hgvs": "NM_000138.5:c.2638G>A"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000325527.5:p.Gly880Ser"
          },
          "RefSeq": {
            "hgvs": "NP_000129.3:p.Gly880Ser"
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}