HGVS | Genome Assembly |
---|---|
NC_000017.11:g.58280369T>A , CM000679.2:g.58280369T>A | GRCh38 |
NC_000017.10:g.56357730T>A , CM000679.1:g.56357730T>A | GRCh37 |
NC_000017.9:g.53712729T>A | NCBI36 |
NG_009629.1:g.5567A>T , LRG_84:g.5567A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000225275.4:c.245A>T MANE Select | ENSP00000225275.3:p.Glu82Val | |
ENST00000225275.3:c.245A>T | ENSP00000225275.3:p.Glu82Val | |
ENST00000580005.1:n.174A>T | ||
NM_000250.1:c.245A>T , LRG_84t1:c.245A>T | NP_000241.1:p.Glu82Val | |
XM_011524821.1:c.431A>T | XP_011523123.1:p.Glu144Val | |
XM_011524822.1:c.-38+236A>T | XP_011523124.1:n.-38+236A>T | |
XM_011524823.1:c.431A>T | XP_011523125.1:p.Glu144Val | |
NM_000250.2:c.245A>T MANE Select | NP_000241.1:p.Glu82Val |