HGVS | Genome Assembly |
---|---|
NC_000001.11:g.67259308T>C , CM000663.2:g.67259308T>C | GRCh38 |
NC_000001.10:g.67724991T>C , CM000663.1:g.67724991T>C | GRCh37 |
NC_000001.9:g.67497579T>C | NCBI36 |
NG_011498.1:g.97823T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000347310.10:c.*180T>C MANE Select | ENSP00000321345.5:n.*180T>C | |
ENST00000347310.9:c.*180T>C | ENSP00000321345.5:n.*180T>C | |
ENST00000395227.2:c.*180T>C | ENSP00000378652.2:n.*180T>C | |
ENST00000473881.2:c.*896T>C | ENSP00000486667.1:n.*896T>C | |
NM_144701.2:c.*180T>C | NP_653302.2:n.*180T>C | |
XM_005270516.2:c.*180T>C | XP_005270573.1:n.*180T>C | |
XM_011540789.1:c.*180T>C | XP_011539091.1:n.*180T>C | |
XM_011540790.1:c.*180T>C | XP_011539092.1:n.*180T>C | |
XM_011540791.1:c.*180T>C | XP_011539093.1:n.*180T>C | |
XM_011540790.3:c.*180T>C | XP_011539092.1:n.*180T>C | |
XM_011540791.3:c.*180T>C | XP_011539093.1:n.*180T>C | |
NM_144701.3:c.*180T>C MANE Select | NP_653302.2:n.*180T>C |