HGVS | Genome Assembly |
---|---|
NC_000017.11:g.44352042T>A , CM000679.2:g.44352042T>A | GRCh38 |
NC_000017.10:g.42429410T>A , CM000679.1:g.42429410T>A | GRCh37 |
NC_000017.9:g.39784936T>A | NCBI36 |
NG_007886.1:g.11920T>A , LRG_661:g.11920T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000053867.8:c.1207T>A MANE Select | ENSP00000053867.2:p.Cys403Ser | |
ENST00000639447.1:c.1136+290T>A | ENSP00000492014.1:n.1136+290T>A | |
ENST00000053867.7:c.1207T>A | ENSP00000053867.2:p.Cys403Ser | |
ENST00000586443.1:c.648T>A | ||
ENST00000589265.5:c.736T>A | ENSP00000467616.1:p.Cys246Ser | |
NM_002087.3:c.1207T>A | NP_002078.1:p.Cys403Ser | |
XM_005257253.1:c.1207T>A | XP_005257310.1:p.Cys403Ser | |
XM_024450730.1:c.1207T>A | XP_024306498.1:p.Cys403Ser | |
NM_002087.4:c.1207T>A MANE Select | NP_002078.1:p.Cys403Ser |