HGVS | Genome Assembly |
---|---|
NC_000019.10:g.38485988C>A , CM000681.2:g.38485988C>A | GRCh38 |
NC_000019.9:g.38976628C>A , CM000681.1:g.38976628C>A | GRCh37 |
NC_000019.8:g.43668468C>A | NCBI36 |
NG_008866.1:g.57289C>A , LRG_766:g.57289C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000599547.6:c.5333C>A | ENSP00000471601.2:p.Ser1778Ter | |
ENST00000359596.8:c.5333C>A MANE Select | ENSP00000352608.2:p.Ser1778Ter | |
ENST00000355481.8:c.5333C>A | ENSP00000347667.3:p.Ser1778Ter | |
ENST00000359596.7:c.5333C>A | ENSP00000352608.2:p.Ser1778Ter | |
ENST00000360985.7:c.5330C>A | ENSP00000354254.4:p.Ser1777Ter | |
NM_000540.2:c.5333C>A , LRG_766t1:c.5333C>A | NP_000531.2:p.Ser1778Ter | |
NM_001042723.1:c.5333C>A | NP_001036188.1:p.Ser1778Ter | |
XM_006723317.1:c.5333C>A | XP_006723380.1:p.Ser1778Ter | |
XM_006723319.1:c.5333C>A | XP_006723382.1:p.Ser1778Ter | |
XM_011527204.1:c.5330C>A | XP_011525506.1:p.Ser1777Ter | |
XM_011527205.1:c.5333C>A | XP_011525507.1:p.Ser1778Ter | |
XM_006723317.2:c.5333C>A | XP_006723380.1:p.Ser1778Ter | |
XM_006723319.2:c.5333C>A | XP_006723382.1:p.Ser1778Ter | |
XM_011527205.2:c.5333C>A | XP_011525507.1:p.Ser1778Ter | |
XR_001753735.1:n.5416C>A | ||
NM_000540.3:c.5333C>A MANE Select | NP_000531.2:p.Ser1778Ter | |
NM_001042723.2:c.5333C>A | NP_001036188.1:p.Ser1778Ter |