HGVS | Genome Assembly |
---|---|
NC_000005.10:g.78955440G>C , CM000667.2:g.78955440G>C | GRCh38 |
NC_000005.9:g.78251263G>C , CM000667.1:g.78251263G>C | GRCh37 |
NC_000005.8:g.78287019G>C | NCBI36 |
NG_007089.1:g.36095C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264914.10:c.753C>G MANE Select | ENSP00000264914.4:p.Tyr251Ter | |
ENST00000565165.2:c.753C>G | ENSP00000456339.2:p.Tyr251Ter | |
ENST00000264914.8:c.753C>G | ENSP00000264914.4:p.Tyr251Ter | |
ENST00000396151.7:c.753C>G | ENSP00000379455.3:p.Tyr251Ter | |
ENST00000565165.1:c.753C>G | ENSP00000456339.1:p.Tyr251Ter | |
NM_000046.3:c.753C>G | NP_000037.2:p.Tyr251Ter | |
NM_198709.2:c.753C>G | NP_942002.1:p.Tyr251Ter | |
XM_005248506.3:c.753C>G | XP_005248563.1:p.Tyr251Ter | |
XM_006714615.2:c.753C>G | XP_006714678.1:p.Tyr251Ter | |
XM_011543390.1:c.753C>G | XP_011541692.1:p.Tyr251Ter | |
XM_011543391.1:c.753C>G | XP_011541693.1:p.Tyr251Ter | |
XM_011543392.1:c.753C>G | XP_011541694.1:p.Tyr251Ter | |
XM_011543393.1:c.753C>G | XP_011541695.1:p.Tyr251Ter | |
NM_000046.4:c.753C>G | NP_000037.2:p.Tyr251Ter | |
XM_011543391.3:c.753C>G | XP_011541693.1:p.Tyr251Ter | |
XM_011543392.3:c.753C>G | XP_011541694.1:p.Tyr251Ter | |
XM_011543393.2:c.753C>G | XP_011541695.1:p.Tyr251Ter | |
XM_017009471.2:c.753C>G | XP_016864960.1:p.Tyr251Ter | |
XR_001742065.2:n.824C>G | ||
XR_001742066.2:n.824C>G | ||
NM_000046.5:c.753C>G MANE Select | NP_000037.2:p.Tyr251Ter | |
NM_198709.3:c.753C>G | NP_942002.1:p.Tyr251Ter |