HGVS | Genome Assembly |
---|---|
NC_000009.12:g.38396509A>T , CM000671.2:g.38396509A>T | GRCh38 |
NC_000009.11:g.38396506A>T , CM000671.1:g.38396506A>T | GRCh37 |
NC_000009.10:g.38386506A>T | NCBI36 |
NG_012253.1:g.8805A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377698.4:c.761A>T MANE Select | ENSP00000366927.3:p.Asp254Val | |
ENST00000377698.3:c.761A>T | ENSP00000366927.3:p.Asp254Val | |
NM_000692.4:c.761A>T | NP_000683.3:p.Asp254Val | |
XM_011517802.1:c.761A>T | XP_011516104.1:p.Asp254Val | |
XM_011517802.2:c.761A>T | XP_011516104.1:p.Asp254Val | |
NM_000692.5:c.761A>T MANE Select | NP_000683.3:p.Asp254Val |