HGVS | Genome Assembly |
---|---|
NC_000001.11:g.36820825G= , CM000663.2:g.36820825G= | GRCh38 |
NC_000001.10:g.37286426G= , CM000663.1:g.37286426G= | GRCh37 |
NC_000001.9:g.37059013G= | NCBI36 |
NG_011447.1:g.218419C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000373091.8:c.1755-971C= MANE Select | ENSP00000362183.3:n.1755-971C= | |
ENST00000373091.7:c.1755-971C= | ENSP00000362183.3:n.1755-971C= | |
ENST00000373093.4:c.1755-971C= | ENSP00000362185.4:n.1755-971C= | |
NM_000831.3:c.1755-971C= | NP_000822.2:n.1755-971C= | |
XM_011541294.1:c.*1690C= | XP_011539596.1:n.*1690C= | |
XM_011541295.1:c.660-971C= | XP_011539597.1:n.660-971C= | |
NM_000831.4:c.1755-971C= MANE Select | NP_000822.2:n.1755-971C= |