HGVS | Genome Assembly |
---|---|
NC_000022.11:g.50489914A>G , CM000684.2:g.50489914A>G | GRCh38 |
NC_000022.10:g.50928343A>G , CM000684.1:g.50928343A>G | GRCh37 |
NC_000022.9:g.49275209A>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000216075.11:c.*58A>G MANE Select | ENSP00000216075.6:n.*58A>G | |
ENST00000216075.10:c.*58A>G | ENSP00000216075.6:n.*58A>G | |
ENST00000395732.7:c.*89A>G | ENSP00000379081.3:n.*89A>G | |
ENST00000395733.7:c.*89A>G | ENSP00000379082.3:n.*89A>G | |
ENST00000451761.1:c.856A>G | ENSP00000409894.1:n.856A>G | |
NM_017584.5:c.*58A>G | NP_060054.4:n.*58A>G | |
XM_005261925.3:c.*58A>G | XP_005261982.1:n.*58A>G | |
XR_244455.2:n.3412A>G | ||
XM_005261925.4:c.*58A>G | XP_005261982.1:n.*58A>G | |
NM_017584.6:c.*58A>G MANE Select | NP_060054.4:n.*58A>G |