HGVS | Genome Assembly |
---|---|
NC_000004.12:g.47406597T= , CM000666.2:g.47406597T= | GRCh38 |
NC_000004.11:g.47408614T= , CM000666.1:g.47408614T= | GRCh37 |
NC_000004.10:g.47103371T= | NCBI36 |
NG_051831.1:g.380320T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295454.8:c.836-85T= MANE Select | ENSP00000295454.3:n.836-85T= | |
ENST00000295454.7:c.836-85T= | ENSP00000295454.3:n.836-85T= | |
NM_000812.3:c.836-85T= | NP_000803.2:n.836-85T= | |
XM_011513678.1:c.815-85T= | XP_011511980.1:n.815-85T= | |
XM_017007985.1:c.185-85T= | XP_016863474.1:n.185-85T= | |
XM_024453976.1:c.737-85T= | XP_024309744.1:n.737-85T= | |
XM_024453977.1:c.737-85T= | XP_024309745.1:n.737-85T= | |
XM_024453978.1:c.737-85T= | XP_024309746.1:n.737-85T= | |
NM_000812.4:c.836-85T= MANE Select | NP_000803.2:n.836-85T= |