HGVS | Genome Assembly |
---|---|
NC_000001.11:g.229432402T>G , CM000663.2:g.229432402T>G | GRCh38 |
NC_000001.10:g.229568149T>G , CM000663.1:g.229568149T>G | GRCh37 |
NC_000001.9:g.227634772T>G | NCBI36 |
NG_006672.1:g.6695A>C , LRG_429:g.6695A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000366683.4:c.484A>C | ENSP00000355644.4:p.Thr162Pro | |
ENST00000684723.1:c.349A>C | ENSP00000508084.1:p.Thr117Pro | |
ENST00000366683.3:c.479+5A>C | ENSP00000355644.3:n.479+5A>C | |
ENST00000366684.7:c.484A>C MANE Select | ENSP00000355645.3:p.Thr162Pro | |
NM_001100.3:c.484A>C , LRG_429t1:c.484A>C | NP_001091.1:p.Thr162Pro | |
NM_001100.4:c.484A>C MANE Select | NP_001091.1:p.Thr162Pro |