HGVS | Genome Assembly |
---|---|
NC_000022.11:g.49913700A= , CM000684.2:g.49913700A= | GRCh38 |
NC_000022.10:g.50307348A= , CM000684.1:g.50307348A= | GRCh37 |
NC_000022.9:g.48693352A= | NCBI36 |
NG_008927.1:g.9759T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000330817.11:c.66T= MANE Select | ENSP00000333813.5:p.Thr22= | |
ENST00000330817.10:c.66T= | ENSP00000333813.5:p.Thr22= | |
NM_024105.3:c.66T= | NP_077010.1:p.Thr22= | |
XM_011530369.1:c.66T= | XP_011528671.1:p.Thr22= | |
XM_011530370.1:c.66T= | XP_011528672.1:p.Thr22= | |
XM_011530371.1:c.66T= | XP_011528673.1:p.Thr22= | |
XM_011530371.2:c.66T= | XP_011528673.1:p.Thr22= | |
XM_017028936.1:c.66T= | XP_016884425.1:p.Thr22= | |
XM_017028937.1:c.66T= | XP_016884426.1:p.Thr22= | |
NM_024105.4:c.66T= MANE Select | NP_077010.1:p.Thr22= |