HGVS | Genome Assembly |
---|---|
NC_000011.10:g.116832814T>A , CM000673.2:g.116832814T>A | GRCh38 |
NC_000011.9:g.116703530T>A , CM000673.1:g.116703530T>A | GRCh37 |
NC_000011.8:g.116208740T>A | NCBI36 |
NG_008949.1:g.7907T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000227667.8:c.230T>A MANE Select | ENSP00000227667.2:p.Val77Asp | |
ENST00000227667.7:c.230T>A | ENSP00000227667.2:p.Val77Asp | |
ENST00000375345.3:c.284T>A | ENSP00000364494.1:p.Val95Asp | |
ENST00000630701.1:c.284T>A | ENSP00000486182.1:p.Val95Asp | |
NM_000040.1:c.230T>A | NP_000031.1:p.Val77Asp | |
NM_000040.2:c.230T>A | NP_000031.1:p.Val77Asp | |
NM_000040.3:c.230T>A MANE Select | NP_000031.1:p.Val77Asp |