HGVS | Genome Assembly |
---|---|
NC_000022.11:g.50489922C= , CM000684.2:g.50489922C= | GRCh38 |
NC_000022.10:g.50928351C= , CM000684.1:g.50928351C= | GRCh37 |
NC_000022.9:g.49275217C= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000216075.11:c.*66C= MANE Select | ENSP00000216075.6:n.*66C= | |
ENST00000216075.10:c.*66C= | ENSP00000216075.6:n.*66C= | |
ENST00000395732.7:c.*97C= | ENSP00000379081.3:n.*97C= | |
ENST00000395733.7:c.*97C= | ENSP00000379082.3:n.*97C= | |
ENST00000451761.1:c.864C= | ENSP00000409894.1:n.864C= | |
NM_017584.5:c.*66C= | NP_060054.4:n.*66C= | |
XM_005261925.3:c.*66C= | XP_005261982.1:n.*66C= | |
XR_244455.2:n.3420C= | ||
XM_005261925.4:c.*66C= | XP_005261982.1:n.*66C= | |
NM_017584.6:c.*66C= MANE Select | NP_060054.4:n.*66C= |