HGVS | Genome Assembly |
---|---|
NC_000017.11:g.50185595G= , CM000679.2:g.50185595G= | GRCh38 |
NC_000017.10:g.48262956G= , CM000679.1:g.48262956G= | GRCh37 |
NC_000017.9:g.45617955G= | NCBI36 |
NG_007400.1:g.21045C= , LRG_1:g.21045C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000225964.10:c.4302C= MANE Select | ENSP00000225964.6:p.Thr1434= | |
ENST00000225964.9:c.4302C= | ENSP00000225964.5:p.Thr1434= | |
NM_000088.3:c.4302C= , LRG_1t1:c.4302C= | NP_000079.2:p.Thr1434= | |
XM_005257058.3:c.4032C= | XP_005257115.2:p.Thr1344= | |
XM_005257059.3:c.3384C= | XP_005257116.2:p.Thr1128= | |
XM_011524341.1:c.4104C= | XP_011522643.1:p.Thr1368= | |
XM_005257058.4:c.4032C= | XP_005257115.2:p.Thr1344= | |
XM_005257059.4:c.3384C= | XP_005257116.2:p.Thr1128= | |
NM_000088.4:c.4302C= MANE Select | NP_000079.2:p.Thr1434= |