HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169555245T>A , CM000663.2:g.169555245T>A | GRCh38 |
NC_000001.10:g.169524483T>A , CM000663.1:g.169524483T>A | GRCh37 |
NC_000001.9:g.167791107T>A | NCBI36 |
NG_011806.1:g.36287A>T , LRG_553:g.36287A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367797.9:c.1055A>T MANE Select | ENSP00000356771.3:p.Tyr352Phe | |
ENST00000367796.3:c.1055A>T | ENSP00000356770.3:p.Tyr352Phe | |
ENST00000367797.7:c.1055A>T | ENSP00000356771.3:p.Tyr352Phe | |
NM_000130.4:c.1055A>T , LRG_553t1:c.1055A>T | NP_000121.2:p.Tyr352Phe | |
XM_017000660.2:c.644A>T | XP_016856149.1:p.Tyr215Phe | |
NM_000130.5:c.1055A>T MANE Select | NP_000121.2:p.Tyr352Phe |