HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133351972A>T , CM000671.2:g.133351972A>T | GRCh38 |
NC_000009.10:g.135208648A>T | NCBI36 |
NG_008477.1:g.9535T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371974.8:c.844T>A MANE Select | ENSP00000361042.3:p.Ser282Thr | |
ENST00000371974.7:c.844T>A | ENSP00000361042.3:p.Ser282Thr | |
ENST00000437995.1:n.754T>A | ||
ENST00000495952.5:n.834T>A | ||
ENST00000615505.4:c.517T>A | ENSP00000482067.1:p.Ser173Thr | |
NM_001280787.1:c.517T>A | NP_001267716.1:p.Ser173Thr | |
NM_003172.3:c.844T>A | NP_003163.1:p.Ser282Thr | |
XM_011518942.1:c.517T>A | XP_011517244.1:p.Ser173Thr | |
NM_003172.4:c.844T>A MANE Select | NP_003163.1:p.Ser282Thr |