HGVS | Genome Assembly |
---|---|
NC_000021.9:g.43417025T>A , CM000683.2:g.43417025T>A | GRCh38 |
NG_052009.1:g.15108A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270162.8:c.2069A>T MANE Select | ENSP00000270162.6:p.Asp690Val | |
ENST00000270162.6:c.2069A>T | ENSP00000270162.6:p.Asp690Val | |
NM_173354.3:c.2069A>T | NP_775490.2:p.Asp690Val | |
XM_011529474.1:c.1922A>T | XP_011527776.1:p.Asp641Val | |
NM_173354.4:c.2069A>T | NP_775490.2:p.Asp690Val | |
XM_011529474.2:c.1922A>T | XP_011527776.1:p.Asp641Val | |
NM_173354.5:c.2069A>T MANE Select | NP_775490.2:p.Asp690Val |