--- 
- 
  A: 
    hgvsc: 
      - ENST00000355349.4:c.5786C>T
      - ENST00000713768.1:c.5786C>T
      - ENST00000713769.1:c.5786C>T
      - NM_000257.4:c.5786C>T
      - NM_001407004.1:c.5786C>T
      - LRG_384t1:c.5786C>T
    hgvsg: 
      - NC_000014.9:g.23413763G>A
      - LRG_384:g.26899C>T
    hgvsp: 
      - ENSP00000347507.3:p.Thr1929Met
      - ENSP00000519070.1:p.Thr1929Met
      - ENSP00000519071.1:p.Thr1929Met
      - NP_000248.2:p.Thr1929Met
      - NP_001393933.1:p.Thr1929Met
      - LRG_384p1:p.Thr1929Met
    id: 
      - rs730880918
      - CM042432
    input: rs730880918
    spdi: 
      - NC_000014.9:23413762:G:A
      - LRG_384:26898:C:T