HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15540680A>T , CM000681.2:g.15540680A>T | GRCh38 |
NC_000019.9:g.15651491A>T , CM000681.1:g.15651491A>T | GRCh37 |
NC_000019.8:g.15512491A>T | NCBI36 |
NG_007987.1:g.37156A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000269703.8:c.902A>T MANE Select | ENSP00000269703.1:p.Lys301Met | |
ENST00000269703.7:c.902A>T | ENSP00000269703.1:p.Lys301Met | |
ENST00000601005.2:c.902A>T | ENSP00000469866.1:p.Lys301Met | |
NM_173483.3:c.902A>T | NP_775754.2:p.Lys301Met | |
XM_011527692.1:c.902A>T | XP_011525994.1:p.Lys301Met | |
XM_011527693.1:c.902A>T | XP_011525995.1:p.Lys301Met | |
XM_011527692.2:c.902A>T | XP_011525994.1:p.Lys301Met | |
XM_011527693.2:c.902A>T | XP_011525995.1:p.Lys301Met | |
NM_173483.4:c.902A>T MANE Select | NP_775754.2:p.Lys301Met |