HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42911113A>T , CM000679.2:g.42911113A>T | GRCh38 |
NC_000017.10:g.41063130A>T , CM000679.1:g.41063130A>T | GRCh37 |
NC_000017.9:g.38316656A>T | NCBI36 |
NG_011808.1:g.15316A>T , LRG_147:g.15316A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000253801.7:c.761A>T MANE Select | ENSP00000253801.1:p.Asp254Val | |
ENST00000253801.6:c.761A>T | ENSP00000253801.1:p.Asp254Val | |
ENST00000585489.1:c.*153A>T | ENSP00000466202.1:n.*153A>T | |
ENST00000592383.5:c.*153A>T | ENSP00000465958.1:n.*153A>T | |
NM_000151.3:c.761A>T | NP_000142.2:p.Asp254Val | |
NM_001270397.1:c.*153A>T | NP_001257326.1:n.*153A>T | |
NM_000151.4:c.761A>T MANE Select | NP_000142.2:p.Asp254Val | |
NM_001270397.2:c.*153A>T | NP_001257326.1:n.*153A>T |