HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189035011T>A , CM000664.2:g.189035011T>A | GRCh38 |
NC_000002.11:g.189899737T>A , CM000664.1:g.189899737T>A | GRCh37 |
NC_000002.10:g.189607982T>A | NCBI36 |
NG_011799.1:g.149869A>T | |
NG_011799.2:g.149869A>T | |
NG_011799.3:g.195291A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000374866.9:c.4258A>T MANE Select | ENSP00000364000.3:p.Lys1420Ter | |
ENST00000374866.7:c.4258A>T | ENSP00000364000.3:p.Lys1420Ter | |
ENST00000618828.1:c.3097A>T | ENSP00000482184.1:p.Lys1033Ter | |
NM_000393.3:c.4258A>T | NP_000384.2:p.Lys1420Ter | |
XM_011510573.1:c.4120A>T | XP_011508875.1:p.Lys1374Ter | |
NM_000393.4:c.4258A>T | NP_000384.2:p.Lys1420Ter | |
XM_011510573.3:c.4120A>T | XP_011508875.1:p.Lys1374Ter | |
NM_000393.5:c.4258A>T MANE Select | NP_000384.2:p.Lys1420Ter |