HGVS | Genome Assembly |
---|---|
NC_000001.11:g.229432143T>G , CM000663.2:g.229432143T>G | GRCh38 |
NC_000001.10:g.229567890T>G , CM000663.1:g.229567890T>G | GRCh37 |
NC_000001.9:g.227634513T>G | NCBI36 |
NG_006672.1:g.6954A>C , LRG_429:g.6954A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000366683.4:c.659A>C | ENSP00000355644.4:p.Tyr220Ser | |
ENST00000684723.1:c.524A>C | ENSP00000508084.1:p.Tyr175Ser | |
ENST00000366683.3:c.479+264A>C | ENSP00000355644.3:n.479+264A>C | |
ENST00000366684.7:c.659A>C MANE Select | ENSP00000355645.3:p.Tyr220Ser | |
NM_001100.3:c.659A>C , LRG_429t1:c.659A>C | NP_001091.1:p.Tyr220Ser | |
NM_001100.4:c.659A>C MANE Select | NP_001091.1:p.Tyr220Ser |