HGVS | Genome Assembly |
---|---|
NC_000023.11:g.74740759G>A , CM000685.2:g.74740759G>A | GRCh38 |
NC_000023.10:g.73960594G>A , CM000685.1:g.73960594G>A | GRCh37 |
NC_000023.9:g.73877319G>A | NCBI36 |
NG_027726.1:g.189694C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000055682.12:c.3798C>T MANE Select | ENSP00000055682.5:p.Gly1266= | |
ENST00000616200.2:c.3798C>T | ENSP00000480284.1:p.Gly1266= | |
ENST00000642681.2:c.3798C>T | ENSP00000495800.1:p.Gly1266= | |
ENST00000055682.10:c.3798C>T | ENSP00000055682.5:p.Gly1266= | |
ENST00000616200.1:c.3798C>T | ENSP00000480284.1:p.Gly1266= | |
NM_001008537.2:c.3798C>T | NP_001008537.1:p.Gly1266= | |
XM_011530935.1:c.3798C>T | XP_011529237.1:p.Gly1266= | |
NM_001008537.3:c.3798C>T MANE Select | NP_001008537.1:p.Gly1266= |