HGVS | Genome Assembly |
---|---|
NC_000001.11:g.186679425A= , CM000663.2:g.186679425A= | GRCh38 |
NC_000001.10:g.186648557A= , CM000663.1:g.186648557A= | GRCh37 |
NC_000001.9:g.184915180A= | NCBI36 |
NG_028206.2:g.6003T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367468.10:c.66T= MANE Select | ENSP00000356438.5:p.Cys22= | |
ENST00000680451.1:c.66T= | ENSP00000506242.1:p.Cys22= | |
ENST00000681605.1:c.66T= | ENSP00000504900.1:p.Cys22= | |
ENST00000367468.9:c.66T= | ENSP00000356438.5:p.Cys22= | |
ENST00000490885.6:n.199T= | ||
ENST00000559627.1:c.66T= | ENSP00000454130.1:p.Cys22= | |
ENST00000559800.1:n.199T= | ||
NM_000963.3:c.66T= | NP_000954.1:p.Cys22= | |
NM_000963.4:c.66T= MANE Select | NP_000954.1:p.Cys22= |