HGVS | Genome Assembly |
---|---|
NC_000022.11:g.50489916G>T , CM000684.2:g.50489916G>T | GRCh38 |
NC_000022.10:g.50928345G>T , CM000684.1:g.50928345G>T | GRCh37 |
NC_000022.9:g.49275211G>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000216075.11:c.*60G>T MANE Select | ENSP00000216075.6:n.*60G>T | |
ENST00000216075.10:c.*60G>T | ENSP00000216075.6:n.*60G>T | |
ENST00000395732.7:c.*91G>T | ENSP00000379081.3:n.*91G>T | |
ENST00000395733.7:c.*91G>T | ENSP00000379082.3:n.*91G>T | |
ENST00000451761.1:c.858G>T | ENSP00000409894.1:n.858G>T | |
NM_017584.5:c.*60G>T | NP_060054.4:n.*60G>T | |
XM_005261925.3:c.*60G>T | XP_005261982.1:n.*60G>T | |
XR_244455.2:n.3414G>T | ||
XM_005261925.4:c.*60G>T | XP_005261982.1:n.*60G>T | |
NM_017584.6:c.*60G>T MANE Select | NP_060054.4:n.*60G>T |