HGVS | Genome Assembly |
---|---|
NC_000008.11:g.133461905C>T , CM000670.2:g.133461905C>T | GRCh38 |
NC_000008.10:g.134474148C>T , CM000670.1:g.134474148C>T | GRCh37 |
NC_000008.9:g.134543330C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000522652.6:c.819G>A MANE Select | ENSP00000430515.1:p.Ser273= | |
ENST00000648219.1:c.819G>A | ENSP00000497381.1:p.Ser273= | |
ENST00000399640.3:c.819G>A | ENSP00000414073.1:p.Ser273= | |
ENST00000521180.5:c.819G>A | ENSP00000428540.1:p.Ser273= | |
ENST00000522652.5:c.819G>A | ENSP00000430515.1:p.Ser273= | |
NM_003033.3:c.819G>A | NP_003024.1:p.Ser273= | |
NM_173344.2:c.819G>A | NP_775479.1:p.Ser273= | |
XM_005251023.1:c.819G>A | XP_005251080.1:p.Ser273= | |
XM_005251024.3:c.819G>A | XP_005251081.1:p.Ser273= | |
XM_005251025.3:c.819G>A | XP_005251082.1:p.Ser273= | |
XM_006716617.1:c.819G>A | XP_006716680.1:p.Ser273= | |
XM_011517225.1:c.819G>A | XP_011515527.1:p.Ser273= | |
XM_011517226.1:c.819G>A | XP_011515528.1:p.Ser273= | |
XM_005251025.5:c.819G>A | XP_005251082.1:p.Ser273= | |
XM_006716617.2:c.819G>A | XP_006716680.1:p.Ser273= | |
XM_011517225.2:c.819G>A | XP_011515527.1:p.Ser273= | |
XM_017013736.2:c.819G>A | XP_016869225.1:p.Ser273= | |
XM_024447233.1:c.819G>A | XP_024303001.1:p.Ser273= | |
NM_173344.3:c.819G>A MANE Select | NP_775479.1:p.Ser273= | |
NM_003033.4:c.819G>A | NP_003024.1:p.Ser273= |