HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73323207T>A , CM000677.2:g.73323207T>A | GRCh38 |
NC_000015.9:g.73615548T>A , CM000677.1:g.73615548T>A | GRCh37 |
NC_000015.8:g.71402601T>A | NCBI36 |
NG_009063.1:g.51058A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.2886A>T MANE Select | ENSP00000261917.3:p.Pro962= | |
ENST00000261917.3:c.2886A>T | ENSP00000261917.3:p.Pro962= | |
NM_005477.2:c.2886A>T | NP_005468.1:p.Pro962= | |
XM_011521148.1:c.1668A>T | XP_011519450.1:p.Pro556= | |
XM_011521148.2:c.1668A>T | XP_011519450.1:p.Pro556= | |
NM_005477.3:c.2886A>T MANE Select | NP_005468.1:p.Pro962= |