HGVS | Genome Assembly |
---|---|
NC_000001.11:g.229432339C>G , CM000663.2:g.229432339C>G | GRCh38 |
NC_000001.10:g.229568086C>G , CM000663.1:g.229568086C>G | GRCh37 |
NC_000001.9:g.227634709C>G | NCBI36 |
NG_006672.1:g.6758G>C , LRG_429:g.6758G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000366683.4:c.547G>C | ENSP00000355644.4:p.Ala183Pro | |
ENST00000684723.1:c.412G>C | ENSP00000508084.1:p.Ala138Pro | |
ENST00000366683.3:c.479+68G>C | ENSP00000355644.3:n.479+68G>C | |
ENST00000366684.7:c.547G>C MANE Select | ENSP00000355645.3:p.Ala183Pro | |
NM_001100.3:c.547G>C , LRG_429t1:c.547G>C | NP_001091.1:p.Ala183Pro | |
NM_001100.4:c.547G>C MANE Select | NP_001091.1:p.Ala183Pro |