HGVS | Genome Assembly |
---|---|
NC_000011.10:g.17386914A= , CM000673.2:g.17386914A= | GRCh38 |
NC_000011.9:g.17408461A= , CM000673.1:g.17408461A= | GRCh37 |
NC_000011.8:g.17365037A= | NCBI36 |
NG_012446.1:g.6746T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682350.1:c.*5T= | ENSP00000508090.1:n.*5T= | |
ENST00000682764.1:c.*5T= | ENSP00000506780.1:n.*5T= | |
ENST00000339994.5:c.*5T= MANE Select | ENSP00000345708.4:n.*5T= | |
ENST00000339994.4:c.*5T= | ENSP00000345708.4:n.*5T= | |
ENST00000528731.1:c.*5T= | ENSP00000434755.1:n.*5T= | |
NM_000525.3:c.*5T= | NP_000516.3:n.*5T= | |
NM_001166290.1:c.*5T= | NP_001159762.1:n.*5T= | |
XM_006718226.2:c.*5T= | XP_006718289.1:n.*5T= | |
XR_930867.1:n.1336T= | ||
XM_006718226.3:c.*5T= | XP_006718289.1:n.*5T= | |
XM_017017680.1:c.*5T= | XP_016873169.1:n.*5T= | |
NM_001166290.2:c.*5T= | NP_001159762.1:n.*5T= | |
NM_001377296.1:c.*5T= | NP_001364225.1:n.*5T= | |
NM_001377297.1:c.*5T= | NP_001364226.1:n.*5T= | |
NM_000525.4:c.*5T= MANE Select | NP_000516.3:n.*5T= |