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