HGVS | Genome Assembly |
---|---|
NC_000015.10:g.65029546C>A , CM000677.2:g.65029546C>A | GRCh38 |
NC_000015.9:g.65321884C>A , CM000677.1:g.65321884C>A | GRCh37 |
NC_000015.8:g.63108937C>A | NCBI36 |
NG_029184.1:g.5094G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000220058.9:c.68G>T MANE Select | ENSP00000220058.4:p.Ser23Ile | |
ENST00000220058.8:c.68G>T | ENSP00000220058.4:p.Ser23Ile | |
ENST00000543678.1:c.68G>T | ENSP00000443754.1:p.Ser23Ile | |
ENST00000558460.5:c.68G>T | ENSP00000452646.1:p.Ser23Ile | |
ENST00000558614.1:n.29G>T | ||
ENST00000560717.5:c.53G>T | ENSP00000457257.1:p.Ser18Ile | |
NM_139242.3:c.68G>T | NP_640335.2:p.Ser23Ile | |
XM_005254158.5:c.68G>T | XP_005254215.2:p.Ser23Ile | |
XR_001751081.1:n.83G>T | ||
NM_139242.4:c.68G>T MANE Select | NP_640335.2:p.Ser23Ile |