HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169541848T>A , CM000663.2:g.169541848T>A | GRCh38 |
NC_000001.10:g.169511086T>A , CM000663.1:g.169511086T>A | GRCh37 |
NC_000001.9:g.167777710T>A | NCBI36 |
NG_011806.1:g.49684A>T , LRG_553:g.49684A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367797.9:c.3242A>T MANE Select | ENSP00000356771.3:p.Asp1081Val | |
ENST00000367796.3:c.3257A>T | ENSP00000356770.3:p.Asp1086Val | |
ENST00000367797.7:c.3242A>T | ENSP00000356771.3:p.Asp1081Val | |
NM_000130.4:c.3242A>T , LRG_553t1:c.3242A>T | NP_000121.2:p.Asp1081Val | |
XM_017000660.2:c.2831A>T | XP_016856149.1:p.Asp944Val | |
NM_000130.5:c.3242A>T MANE Select | NP_000121.2:p.Asp1081Val |