HGVS | Genome Assembly |
---|---|
NC_000009.12:g.77794491T>A , CM000671.2:g.77794491T>A | GRCh38 |
NC_000009.11:g.80409407T>A , CM000671.1:g.80409407T>A | GRCh37 |
NC_000009.10:g.79599227T>A | NCBI36 |
NG_027904.2:g.241813A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286548.9:c.707A>T MANE Select | ENSP00000286548.4:p.Asp236Val | |
ENST00000286548.8:c.707A>T | ENSP00000286548.4:p.Asp236Val | |
NM_002072.4:c.707A>T | NP_002063.2:p.Asp236Val | |
XM_017014628.2:c.533A>T | XP_016870117.1:p.Asp178Val | |
NM_002072.5:c.707A>T MANE Select | NP_002063.2:p.Asp236Val |