HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42901082A>T , CM000679.2:g.42901082A>T | GRCh38 |
NC_000017.10:g.41053099A>T , CM000679.1:g.41053099A>T | GRCh37 |
NC_000017.9:g.38306625A>T | NCBI36 |
NG_011808.1:g.5285A>T , LRG_147:g.5285A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000253801.7:c.206A>T MANE Select | ENSP00000253801.1:p.Asp69Val | |
ENST00000253801.6:c.206A>T | ENSP00000253801.1:p.Asp69Val | |
ENST00000585489.1:c.206A>T | ENSP00000466202.1:p.Asp69Val | |
ENST00000588481.1:n.271A>T | ||
ENST00000592383.5:c.206A>T | ENSP00000465958.1:p.Asp69Val | |
NM_000151.3:c.206A>T | NP_000142.2:p.Asp69Val | |
NM_001270397.1:c.206A>T | NP_001257326.1:p.Asp69Val | |
NM_000151.4:c.206A>T MANE Select | NP_000142.2:p.Asp69Val | |
NM_001270397.2:c.206A>T | NP_001257326.1:p.Asp69Val |