HGVS | Genome Assembly |
---|---|
NC_000004.12:g.47406718C>G , CM000666.2:g.47406718C>G | GRCh38 |
NC_000004.11:g.47408735C>G , CM000666.1:g.47408735C>G | GRCh37 |
NC_000004.10:g.47103492C>G | NCBI36 |
NG_051831.1:g.380441C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000295454.8:c.872C>G MANE Select | ENSP00000295454.3:p.Thr291Ser | |
ENST00000295454.7:c.872C>G | ENSP00000295454.3:p.Thr291Ser | |
NM_000812.3:c.872C>G | NP_000803.2:p.Thr291Ser | |
XM_011513678.1:c.851C>G | XP_011511980.1:p.Thr284Ser | |
XM_017007985.1:c.221C>G | XP_016863474.1:p.Thr74Ser | |
XM_024453976.1:c.773C>G | XP_024309744.1:p.Thr258Ser | |
XM_024453977.1:c.773C>G | XP_024309745.1:p.Thr258Ser | |
XM_024453978.1:c.773C>G | XP_024309746.1:p.Thr258Ser | |
NM_000812.4:c.872C>G MANE Select | NP_000803.2:p.Thr291Ser |