HGVS | Genome Assembly |
---|---|
NC_000001.11:g.102998319A>T , CM000663.2:g.102998319A>T | GRCh38 |
NC_000001.10:g.103463875A>T , CM000663.1:g.103463875A>T | GRCh37 |
NC_000001.9:g.103236463A>T | NCBI36 |
NG_008033.1:g.115178T>A | |
NG_008033.2:g.115178T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370096.9:c.2187T>A MANE Select | ENSP00000359114.3:p.Asp729Glu | |
ENST00000353414.8:c.2070T>A | ENSP00000302551.6:p.Asp690Glu | |
ENST00000358392.6:c.2223T>A | ENSP00000351163.2:p.Asp741Glu | |
ENST00000370096.7:c.2187T>A | ENSP00000359114.3:p.Asp729Glu | |
ENST00000512756.5:c.1839T>A | ENSP00000426533.1:p.Asp613Glu | |
ENST00000635193.1:c.1505T>A | ||
NM_001190709.1:c.2070T>A | NP_001177638.1:p.Asp690Glu | |
NM_001854.3:c.2187T>A | NP_001845.3:p.Asp729Glu | |
NM_080629.2:c.2223T>A | NP_542196.2:p.Asp741Glu | |
NM_080630.3:c.1839T>A | NP_542197.3:p.Asp613Glu | |
XM_011540719.1:c.2187T>A | XP_011539021.1:p.Asp729Glu | |
XM_011540720.1:c.420T>A | XP_011539022.1:p.Asp140Glu | |
XM_011540721.1:c.-242T>A | XP_011539023.1:n.-242T>A | |
XR_946545.1:n.2585T>A | ||
NR_134980.1:n.2505T>A | ||
XM_017000334.1:c.2340T>A | XP_016855823.1:p.Asp780Glu | |
XM_017000335.1:c.2334T>A | XP_016855824.1:p.Asp778Glu | |
XM_017000336.1:c.2340T>A | XP_016855825.1:p.Asp780Glu | |
XM_017000337.1:c.738T>A | XP_016855826.1:p.Asp246Glu | |
NM_001854.4:c.2187T>A MANE Select | NP_001845.3:p.Asp729Glu | |
NM_080630.4:c.1839T>A | NP_542197.3:p.Asp613Glu | |
NR_134980.2:n.2531T>A | ||
NM_001190709.2:c.2070T>A | NP_001177638.1:p.Asp690Glu | |
NM_080629.3:c.2223T>A | NP_542196.2:p.Asp741Glu |