HGVS | Genome Assembly |
---|---|
NC_000017.11:g.7454399T>G , CM000679.2:g.7454399T>G | GRCh38 |
NC_000017.10:g.7357718T>G , CM000679.1:g.7357718T>G | GRCh37 |
NC_000017.9:g.7298442T>G | NCBI36 |
NG_008026.1:g.14313T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000306071.7:c.923T>G MANE Select | ENSP00000304290.2:p.Ile308Ser | |
ENST00000306071.6:c.923T>G | ENSP00000304290.2:p.Ile308Ser | |
ENST00000536404.6:c.707T>G | ENSP00000439209.2:p.Ile236Ser | |
ENST00000570557.5:c.586T>G | ||
ENST00000573209.1:n.1867T>G | ||
ENST00000576360.1:c.605-45T>G | ENSP00000459092.1:n.605-45T>G | |
NM_000747.2:c.923T>G | NP_000738.2:p.Ile308Ser | |
NM_000747.3:c.923T>G MANE Select | NP_000738.2:p.Ile308Ser |