HGVS | Genome Assembly |
---|---|
NC_000022.11:g.50489912A>G , CM000684.2:g.50489912A>G | GRCh38 |
NC_000022.10:g.50928341A>G , CM000684.1:g.50928341A>G | GRCh37 |
NC_000022.9:g.49275207A>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000216075.11:c.*56A>G MANE Select | ENSP00000216075.6:n.*56A>G | |
ENST00000216075.10:c.*56A>G | ENSP00000216075.6:n.*56A>G | |
ENST00000395732.7:c.*87A>G | ENSP00000379081.3:n.*87A>G | |
ENST00000395733.7:c.*87A>G | ENSP00000379082.3:n.*87A>G | |
ENST00000451761.1:c.854A>G | ENSP00000409894.1:n.854A>G | |
NM_017584.5:c.*56A>G | NP_060054.4:n.*56A>G | |
XM_005261925.3:c.*56A>G | XP_005261982.1:n.*56A>G | |
XR_244455.2:n.3410A>G | ||
XM_005261925.4:c.*56A>G | XP_005261982.1:n.*56A>G | |
NM_017584.6:c.*56A>G MANE Select | NP_060054.4:n.*56A>G |