HGVS | Genome Assembly |
---|---|
NC_000005.10:g.93585387T>A , CM000667.2:g.93585387T>A | GRCh38 |
NC_000005.9:g.92921093T>A , CM000667.1:g.92921093T>A | GRCh37 |
NC_000005.8:g.92946849T>A | NCBI36 |
NG_034119.1:g.7051T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000615873.2:c.289T>A | ENSP00000481517.1:p.Cys97Ser | |
ENST00000327111.8:c.364T>A MANE Select | ENSP00000325819.3:p.Cys122Ser | |
ENST00000647447.1:c.211T>A | ENSP00000495740.1:p.Cys71Ser | |
ENST00000327111.7:c.364T>A | ENSP00000325819.3:p.Cys122Ser | |
ENST00000615873.1:c.289T>A | ENSP00000481517.1:p.Cys97Ser | |
NM_005654.5:c.364T>A | NP_005645.1:p.Cys122Ser | |
NM_005654.6:c.364T>A MANE Select | NP_005645.1:p.Cys122Ser |