HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3154675A>T , CM000668.2:g.3154675A>T | GRCh38 |
NC_000006.11:g.3154909A>T , CM000668.1:g.3154909A>T | GRCh37 |
NC_000006.10:g.3099908A>T | NCBI36 |
NG_042223.1:g.7875T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000333628.4:c.526T>A MANE Select | ENSP00000369703.2:p.Ser176Thr | |
ENST00000679400.1:n.582T>A | ||
ENST00000679907.1:n.914T>A | ||
ENST00000680036.1:n.1308T>A | ||
ENST00000680967.1:n.1616T>A | ||
ENST00000333628.3:c.526T>A | ENSP00000369703.2:p.Ser176Thr | |
ENST00000489942.1:n.721T>A | ||
NM_001069.2:c.526T>A | NP_001060.1:p.Ser176Thr | |
NM_001310315.1:c.271T>A | NP_001297244.1:p.Ser91Thr | |
NM_001069.3:c.526T>A MANE Select | NP_001060.1:p.Ser176Thr | |
NM_001310315.2:c.271T>A | NP_001297244.1:p.Ser91Thr |