HGVS | Genome Assembly |
---|---|
NC_000011.10:g.121307159T= , CM000673.2:g.121307159T= | GRCh38 |
NC_000011.9:g.121177868T= , CM000673.1:g.121177868T= | GRCh37 |
NC_000011.8:g.120683078T= | NCBI36 |
NG_009446.1:g.19481T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264027.9:c.547T= MANE Select | ENSP00000264027.4:p.Tyr183= | |
ENST00000264027.8:c.547T= | ENSP00000264027.4:p.Tyr183= | |
ENST00000392789.2:c.547T= | ENSP00000376539.2:p.Tyr183= | |
ENST00000527183.1:n.840T= | ||
ENST00000528991.1:n.240T= | ||
ENST00000534230.5:c.547T= | ENSP00000432550.1:p.Tyr183= | |
NM_001024956.2:c.547T= | NP_001020127.1:p.Tyr183= | |
NM_006918.4:c.547T= | NP_008849.2:p.Tyr183= | |
NM_006918.5:c.547T= MANE Select | NP_008849.2:p.Tyr183= | |
NM_001024956.3:c.547T= | NP_001020127.1:p.Tyr183= |