HGVS | Genome Assembly |
---|---|
NC_000010.11:g.95614027G>A , CM000672.2:g.95614027G>A | GRCh38 |
NC_000010.10:g.97373784G>A , CM000672.1:g.97373784G>A | GRCh37 |
NC_000010.9:g.97363774G>A | NCBI36 |
NG_012258.1:g.47784C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371224.7:c.1740C>T MANE Select | ENSP00000360268.2:p.Ser580= | |
ENST00000371221.3:c.1734C>T | ENSP00000360265.3:p.Ser578= | |
ENST00000371224.6:c.1740C>T | ENSP00000360268.2:p.Ser580= | |
ENST00000485428.1:n.356C>T | ||
NM_001017423.1:c.1734C>T | NP_001017423.1:p.Ser578= | |
NM_002860.3:c.1740C>T | NP_002851.2:p.Ser580= | |
XM_006717933.1:c.1740C>T | XP_006717996.1:p.Ser580= | |
XM_011540001.1:c.1407C>T | XP_011538303.1:p.Ser469= | |
NM_001323412.1:c.1407C>T | NP_001310341.1:p.Ser469= | |
NM_001323413.1:c.1740C>T | NP_001310342.1:p.Ser580= | |
NM_001323414.1:c.1740C>T | NP_001310343.1:p.Ser580= | |
NM_001323415.1:c.1734C>T | NP_001310344.1:p.Ser578= | |
NM_001323416.1:c.1407C>T | NP_001310345.1:p.Ser469= | |
NM_001323417.1:c.1635C>T | NP_001310346.1:p.Ser545= | |
NM_001323418.1:c.1401C>T | NP_001310347.1:p.Ser467= | |
NM_001323419.1:c.1104C>T | NP_001310348.1:p.Ser368= | |
XM_024448094.1:c.1740C>T | XP_024303862.1:p.Ser580= | |
XM_024448095.1:c.1740C>T | XP_024303863.1:p.Ser580= | |
XM_024448096.1:c.1734C>T | XP_024303864.1:p.Ser578= | |
XM_024448097.1:c.1407C>T | XP_024303865.1:p.Ser469= | |
NM_002860.4:c.1740C>T MANE Select | NP_002851.2:p.Ser580= | |
NM_001017423.2:c.1734C>T | NP_001017423.1:p.Ser578= | |
NM_001323412.2:c.1407C>T | NP_001310341.1:p.Ser469= | |
NM_001323413.2:c.1740C>T | NP_001310342.1:p.Ser580= | |
NM_001323414.2:c.1740C>T | NP_001310343.1:p.Ser580= | |
NM_001323415.2:c.1734C>T | NP_001310344.1:p.Ser578= | |
NM_001323416.2:c.1407C>T | NP_001310345.1:p.Ser469= | |
NM_001323417.2:c.1635C>T | NP_001310346.1:p.Ser545= | |
NM_001323418.2:c.1401C>T | NP_001310347.1:p.Ser467= | |
NM_001323419.2:c.1104C>T | NP_001310348.1:p.Ser368= |