HGVS | Genome Assembly |
---|---|
NC_000001.11:g.202596755G= , CM000663.2:g.202596755G= | GRCh38 |
NC_000001.10:g.202565883G= , CM000663.1:g.202565883G= | GRCh37 |
NC_000001.9:g.200832506G= | NCBI36 |
NG_041776.1:g.118669C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367268.5:c.*2C= MANE Select | ENSP00000356237.4:n.*2C= | |
ENST00000367267.5:c.*2C= | ENSP00000356236.1:n.*2C= | |
ENST00000367268.4:c.*2C= | ENSP00000356237.4:n.*2C= | |
NM_001136504.1:c.*2C= | NP_001129976.1:n.*2C= | |
NM_177402.4:c.*2C= | NP_796376.2:n.*2C= | |
XM_011509192.1:c.*2C= | XP_011507494.1:n.*2C= | |
XM_011509192.2:c.*2C= | XP_011507494.1:n.*2C= | |
XM_017000309.2:c.*2C= | XP_016855798.1:n.*2C= | |
XM_017000310.2:c.*2C= | XP_016855799.1:n.*2C= | |
XM_017000311.2:c.*2C= | XP_016855800.1:n.*2C= | |
XM_017000312.1:c.*2C= | XP_016855801.1:n.*2C= | |
XM_017000313.1:c.*2C= | XP_016855802.1:n.*2C= | |
NM_177402.5:c.*2C= MANE Select | NP_796376.2:n.*2C= |