HGVS | Genome Assembly |
---|---|
NC_000004.12:g.47406717A>T , CM000666.2:g.47406717A>T | GRCh38 |
NC_000004.11:g.47408734A>T , CM000666.1:g.47408734A>T | GRCh37 |
NC_000004.10:g.47103491A>T | NCBI36 |
NG_051831.1:g.380440A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000295454.8:c.871A>T MANE Select | ENSP00000295454.3:p.Thr291Ser | |
ENST00000295454.7:c.871A>T | ENSP00000295454.3:p.Thr291Ser | |
NM_000812.3:c.871A>T | NP_000803.2:p.Thr291Ser | |
XM_011513678.1:c.850A>T | XP_011511980.1:p.Thr284Ser | |
XM_017007985.1:c.220A>T | XP_016863474.1:p.Thr74Ser | |
XM_024453976.1:c.772A>T | XP_024309744.1:p.Thr258Ser | |
XM_024453977.1:c.772A>T | XP_024309745.1:p.Thr258Ser | |
XM_024453978.1:c.772A>T | XP_024309746.1:p.Thr258Ser | |
NM_000812.4:c.871A>T MANE Select | NP_000803.2:p.Thr291Ser |