{
  "@context": "http://reg.genome.network/schema/allele.jsonld",
  "@id": "http://reg.genome.network/allele/CA402918918",
  "communityStandardTitle": [
    "NM_001972.4(ELANE):c.618G>C (p.Leu206Phe)"
  ],
  "externalRecords": {
    "ClinVarAlleles": [
      {
        "@id": "http://www.ncbi.nlm.nih.gov/clinvar/?term=791965[alleleid]",
        "alleleId": 791965,
        "preferredName": "NM_001972.4(ELANE):c.618G>C (p.Leu206Phe)"
      }
    ],
    "ClinVarVariations": [
      {
        "@id": "http://www.ncbi.nlm.nih.gov/clinvar/variation/803508",
        "RCV": [
          "RCV000990117"
        ],
        "variationId": 803508
      }
    ],
    "MyVariantInfo_hg19": [
      {
        "@id": "http://myvariant.info/v1/variant/chr19:g.855978G>C?assembly=hg19",
        "id": "chr19:g.855978G>C"
      }
    ],
    "MyVariantInfo_hg38": [
      {
        "@id": "http://myvariant.info/v1/variant/chr19:g.855978G>C?assembly=hg38",
        "id": "chr19:g.855978G>C"
      }
    ],
    "dbSNP": [
      {
        "@id": "http://www.ncbi.nlm.nih.gov/snp/137854446",
        "rs": 137854446
      }
    ]
  },
  "genomicAlleles": [
    {
      "chromosome": "19",
      "coordinates": [
        {
          "allele": "C",
          "end": 855978,
          "referenceAllele": "G",
          "start": 855977
        }
      ],
      "hgvs": [
        "NC_000019.10:g.855978G>C",
        "CM000681.2:g.855978G>C"
      ],
      "referenceGenome": "GRCh38",
      "referenceSequence": "http://reg.genome.network/refseq/RS000067"
    },
    {
      "chromosome": "19",
      "coordinates": [
        {
          "allele": "C",
          "end": 855978,
          "referenceAllele": "G",
          "start": 855977
        }
      ],
      "hgvs": [
        "NC_000019.9:g.855978G>C",
        "CM000681.1:g.855978G>C"
      ],
      "referenceGenome": "GRCh37",
      "referenceSequence": "http://reg.genome.network/refseq/RS000043"
    },
    {
      "chromosome": "19",
      "coordinates": [
        {
          "allele": "C",
          "end": 806978,
          "referenceAllele": "G",
          "start": 806977
        }
      ],
      "hgvs": [
        "NC_000019.8:g.806978G>C"
      ],
      "referenceGenome": "NCBI36",
      "referenceSequence": "http://reg.genome.network/refseq/RS000019"
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 1314,
          "referenceAllele": "G",
          "start": 1313
        }
      ],
      "hgvs": [
        "NG_007274.1:g.1314G>C",
        "LRG_46:g.1314G>C"
      ],
      "referenceSequence": "http://reg.genome.network/refseq/RS000522"
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 8688,
          "referenceAllele": "G",
          "start": 8687
        }
      ],
      "hgvs": [
        "NG_009627.1:g.8688G>C",
        "LRG_57:g.8688G>C"
      ],
      "referenceSequence": "http://reg.genome.network/refseq/RS001618"
    }
  ],
  "transcriptAlleles": [
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 644,
          "referenceAllele": "G",
          "start": 643
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003309",
      "geneNCBI_id": 1991,
      "geneSymbol": "ELANE",
      "hgvs": [
        "ENST00000263621.2:c.618G>C"
      ],
      "proteinEffect": {
        "hgvs": "ENSP00000263621.1:p.Leu206Phe",
        "hgvsWellDefined": "ENSP00000263621.1:p.Leu206Phe"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS742533",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000263621.2:c.618G>C"
          },
          "RefSeq": {
            "hgvs": "NM_001972.4:c.618G>C"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000263621.1:p.Leu206Phe"
          },
          "RefSeq": {
            "hgvs": "NP_001963.1:p.Leu206Phe"
          }
        }
      }
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 656,
          "referenceAllele": "G",
          "start": 655
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003309",
      "geneNCBI_id": 1991,
      "geneSymbol": "ELANE",
      "hgvs": [
        "ENST00000263621.1:c.618G>C"
      ],
      "proteinEffect": {
        "hgvs": "ENSP00000263621.1:p.Leu206Phe",
        "hgvsWellDefined": "ENSP00000263621.1:p.Leu206Phe"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS251302"
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 759,
          "referenceAllele": "G",
          "start": 758
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003309",
      "geneNCBI_id": 1991,
      "geneSymbol": "ELANE",
      "hgvs": [
        "ENST00000590230.5:c.618G>C"
      ],
      "proteinEffect": {
        "hgvs": "ENSP00000466090.1:p.Leu206Phe",
        "hgvsWellDefined": "ENSP00000466090.1:p.Leu206Phe"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS392049"
    },
    {
      "@id": "http://reg.genome.network/allele/PA101245",
      "coordinates": [
        {
          "allele": "C",
          "end": 656,
          "referenceAllele": "G",
          "start": 655
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003309",
      "geneNCBI_id": 1991,
      "geneSymbol": "ELANE",
      "hgvs": [
        "NM_001972.2:c.618G>C",
        "LRG_57t1:c.618G>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_001963.1:p.Leu206Phe",
        "hgvsWellDefined": "NP_001963.1:p.Leu206Phe"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS027298"
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 1415,
          "referenceAllele": "G",
          "start": 1414
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003309",
      "geneNCBI_id": 1991,
      "geneSymbol": "ELANE",
      "hgvs": [
        "XM_011527775.1:c.618G>C"
      ],
      "proteinEffect": {
        "hgvs": "XP_011526077.1:p.Leu206Phe",
        "hgvsWellDefined": "XP_011526077.1:p.Leu206Phe"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS094858"
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 754,
          "referenceAllele": "G",
          "start": 753
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003309",
      "geneNCBI_id": 1991,
      "geneSymbol": "ELANE",
      "hgvs": [
        "XM_011527776.1:c.618G>C"
      ],
      "proteinEffect": {
        "hgvs": "XP_011526078.1:p.Leu206Phe",
        "hgvsWellDefined": "XP_011526078.1:p.Leu206Phe"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS094859"
    },
    {
      "@id": "http://reg.genome.network/allele/PA101245",
      "coordinates": [
        {
          "allele": "C",
          "end": 738,
          "referenceAllele": "G",
          "start": 737
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003309",
      "geneNCBI_id": 1991,
      "geneSymbol": "ELANE",
      "hgvs": [
        "NM_001972.3:c.618G>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_001963.1:p.Leu206Phe",
        "hgvsWellDefined": "NP_001963.1:p.Leu206Phe"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS524940"
    },
    {
      "@id": "http://reg.genome.network/allele/PA101245",
      "coordinates": [
        {
          "allele": "C",
          "end": 644,
          "referenceAllele": "G",
          "start": 643
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003309",
      "geneNCBI_id": 1991,
      "geneSymbol": "ELANE",
      "hgvs": [
        "NM_001972.4:c.618G>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_001963.1:p.Leu206Phe",
        "hgvsWellDefined": "NP_001963.1:p.Leu206Phe"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS665281",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000263621.2:c.618G>C"
          },
          "RefSeq": {
            "hgvs": "NM_001972.4:c.618G>C"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000263621.1:p.Leu206Phe"
          },
          "RefSeq": {
            "hgvs": "NP_001963.1:p.Leu206Phe"
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}