HGVS | Genome Assembly |
---|---|
NC_000013.11:g.23886484A= , CM000675.2:g.23886484A= | GRCh38 |
NC_000013.10:g.24460623A= , CM000675.1:g.24460623A= | GRCh37 |
NC_000013.9:g.23358623A= | NCBI36 |
NG_052977.1:g.7965T= |
HGVS | Amino-acid Change |
---|---|
NM_005932.4:c.212T= MANE Select | NP_005923.3:p.Leu71= |
ENST00000382172.4:c.212T= MANE Select | ENSP00000371607.3:p.Leu71= |
NM_005932.3:c.212T= | NP_005923.2:p.Leu71= |
ENST00000382172.3:c.212T= | ENSP00000371607.3:p.Leu71= |
ENST00000469167.1:n.744T= | |
XM_011535097.1:c.26T= | XP_011533399.1:p.Leu9= |
XM_011535097.2:c.26T= | XP_011533399.1:p.Leu9= |
XM_011535098.1:c.212T= | XP_011533400.1:p.Leu71= |
XM_011535098.3:c.212T= | XP_011533400.1:p.Leu71= |