HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31519804T>A , CM000680.2:g.31519804T>A | GRCh38 |
NC_000018.9:g.29099767T>A , CM000680.1:g.29099767T>A | GRCh37 |
NC_000018.8:g.27353765T>A | NCBI36 |
NG_007072.3:g.26563T>A , LRG_397:g.26563T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000682241.2:c.83T>A | ENSP00000507600.2:p.Val28Asp | |
ENST00000683654.1:c.83T>A | ENSP00000506971.1:p.Val28Asp | |
ENST00000261590.13:c.83T>A MANE Select | ENSP00000261590.8:p.Val28Asp | |
ENST00000261590.12:c.83T>A | ENSP00000261590.8:p.Val28Asp | |
ENST00000585206.1:c.83T>A | ENSP00000462503.1:p.Val28Asp | |
NM_001943.3:c.83T>A , LRG_397t1:c.83T>A | NP_001934.2:p.Val28Asp | |
NM_001943.4:c.83T>A | NP_001934.2:p.Val28Asp | |
XM_024451095.1:c.-452T>A | XP_024306863.1:n.-452T>A | |
NM_001943.5:c.83T>A MANE Select | NP_001934.2:p.Val28Asp |