HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15540639T>C , CM000681.2:g.15540639T>C | GRCh38 |
NC_000019.9:g.15651450T>C , CM000681.1:g.15651450T>C | GRCh37 |
NC_000019.8:g.15512450T>C | NCBI36 |
NG_007987.1:g.37115T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000269703.8:c.861T>C MANE Select | ENSP00000269703.1:p.Arg287= | |
ENST00000269703.7:c.861T>C | ENSP00000269703.1:p.Arg287= | |
ENST00000601005.2:c.861T>C | ENSP00000469866.1:p.Arg287= | |
NM_173483.3:c.861T>C | NP_775754.2:p.Arg287= | |
XM_011527692.1:c.861T>C | XP_011525994.1:p.Arg287= | |
XM_011527693.1:c.861T>C | XP_011525995.1:p.Arg287= | |
XM_011527692.2:c.861T>C | XP_011525994.1:p.Arg287= | |
XM_011527693.2:c.861T>C | XP_011525995.1:p.Arg287= | |
NM_173483.4:c.861T>C MANE Select | NP_775754.2:p.Arg287= |