HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7933953G>T , CM000681.2:g.7933953G>T | GRCh38 |
NC_000019.9:g.7998838G>T , CM000681.1:g.7998838G>T | GRCh37 |
NC_000019.8:g.7904838G>T | NCBI36 |
NG_051180.1:g.14871C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270538.8:c.594C>A MANE Select | ENSP00000270538.2:p.Thr198= | |
ENST00000270538.7:c.594C>A | ENSP00000270538.2:p.Thr198= | |
ENST00000595831.5:c.581C>A | ||
ENST00000595876.5:c.*282C>A | ENSP00000471596.1:n.*282C>A | |
ENST00000597926.1:c.498C>A | ENSP00000469389.1:p.Thr166= | |
ENST00000600748.5:n.579C>A | ||
NM_006351.3:c.594C>A | NP_006342.2:p.Thr198= | |
NM_006351.4:c.594C>A MANE Select | NP_006342.2:p.Thr198= |