HGVS | Genome Assembly |
---|---|
NC_000017.11:g.80104578T= , CM000679.2:g.80104578T= | GRCh38 |
NC_000017.10:g.78078377T= , CM000679.1:g.78078377T= | GRCh37 |
NC_000017.9:g.75692972T= | NCBI36 |
NG_009822.1:g.8023T= , LRG_673:g.8023T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000570803.6:c.-9T= | ENSP00000460543.2:n.-9T= | |
ENST00000572080.2:c.-9T= | ENSP00000459972.2:n.-9T= | |
ENST00000577106.6:c.-9T= | ENSP00000458306.2:n.-9T= | |
ENST00000302262.8:c.-9T= MANE Select | ENSP00000305692.3:n.-9T= | |
ENST00000302262.7:c.-9T= | ENSP00000305692.3:n.-9T= | |
ENST00000390015.7:c.-9T= | ENSP00000374665.3:n.-9T= | |
ENST00000570803.5:c.-9T= | ENSP00000460543.1:n.-9T= | |
ENST00000577106.5:c.-9T= | ENSP00000458306.1:n.-9T= | |
NM_000152.3:c.-9T= , LRG_673t1:c.-9T= | NP_000143.2:n.-9T= | |
NM_001079803.1:c.-9T= | NP_001073271.1:n.-9T= | |
NM_001079804.1:c.-9T= | NP_001073272.1:n.-9T= | |
XM_005257193.1:c.-9T= | XP_005257250.1:n.-9T= | |
XM_005257194.3:c.-9T= | XP_005257251.1:n.-9T= | |
NM_000152.4:c.-9T= | NP_000143.2:n.-9T= | |
NM_001079803.2:c.-9T= | NP_001073271.1:n.-9T= | |
NM_001079804.2:c.-9T= | NP_001073272.1:n.-9T= | |
XM_005257193.2:c.-9T= | XP_005257250.1:n.-9T= | |
XM_005257194.4:c.-9T= | XP_005257251.1:n.-9T= | |
NM_000152.5:c.-9T= MANE Select | NP_000143.2:n.-9T= | |
NM_001079803.3:c.-9T= | NP_001073271.1:n.-9T= | |
NM_001079804.3:c.-9T= | NP_001073272.1:n.-9T= |