HGVS | Genome Assembly |
---|---|
NC_000023.11:g.74740762A= , CM000685.2:g.74740762A= | GRCh38 |
NC_000023.10:g.73960597A= , CM000685.1:g.73960597A= | GRCh37 |
NC_000023.9:g.73877322A= | NCBI36 |
NG_027726.1:g.189691T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000055682.12:c.3795T= MANE Select | ENSP00000055682.5:p.Gly1265= | |
ENST00000616200.2:c.3795T= | ENSP00000480284.1:p.Gly1265= | |
ENST00000642681.2:c.3795T= | ENSP00000495800.1:p.Gly1265= | |
ENST00000055682.10:c.3795T= | ENSP00000055682.5:p.Gly1265= | |
ENST00000616200.1:c.3795T= | ENSP00000480284.1:p.Gly1265= | |
NM_001008537.2:c.3795T= | NP_001008537.1:p.Gly1265= | |
XM_011530935.1:c.3795T= | XP_011529237.1:p.Gly1265= | |
NM_001008537.3:c.3795T= MANE Select | NP_001008537.1:p.Gly1265= |