HGVS | Genome Assembly |
---|---|
NC_000001.11:g.36820823A= , CM000663.2:g.36820823A= | GRCh38 |
NC_000001.10:g.37286424A= , CM000663.1:g.37286424A= | GRCh37 |
NC_000001.9:g.37059011A= | NCBI36 |
NG_011447.1:g.218421T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000373091.8:c.1755-969T= MANE Select | ENSP00000362183.3:n.1755-969T= | |
ENST00000373091.7:c.1755-969T= | ENSP00000362183.3:n.1755-969T= | |
ENST00000373093.4:c.1755-969T= | ENSP00000362185.4:n.1755-969T= | |
NM_000831.3:c.1755-969T= | NP_000822.2:n.1755-969T= | |
XM_011541294.1:c.*1692T= | XP_011539596.1:n.*1692T= | |
XM_011541295.1:c.660-969T= | XP_011539597.1:n.660-969T= | |
NM_000831.4:c.1755-969T= MANE Select | NP_000822.2:n.1755-969T= |