HGVS | Genome Assembly |
---|---|
NC_000001.11:g.36820777A>T , CM000663.2:g.36820777A>T | GRCh38 |
NC_000001.10:g.37286378A>T , CM000663.1:g.37286378A>T | GRCh37 |
NC_000001.9:g.37058965A>T | NCBI36 |
NG_011447.1:g.218467T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000373091.8:c.1755-923T>A MANE Select | ENSP00000362183.3:n.1755-923T>A | |
ENST00000373091.7:c.1755-923T>A | ENSP00000362183.3:n.1755-923T>A | |
ENST00000373093.4:c.1755-923T>A | ENSP00000362185.4:n.1755-923T>A | |
NM_000831.3:c.1755-923T>A | NP_000822.2:n.1755-923T>A | |
XM_011541295.1:c.660-923T>A | XP_011539597.1:n.660-923T>A | |
NM_000831.4:c.1755-923T>A MANE Select | NP_000822.2:n.1755-923T>A |