HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20425828G= , CM000684.2:g.20425828G= | GRCh38 |
NC_000022.10:g.20780115G= , CM000684.1:g.20780115G= | GRCh37 |
NC_000022.9:g.19110115G= | NCBI36 |
NG_031868.2:g.17032C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000622235.5:c.2148C= MANE Select | ENSP00000477564.2:p.Thr716= | |
ENST00000615031.4:c.2163C= | ENSP00000479389.1:p.Thr721= | |
ENST00000622235.4:c.2148C= | ENSP00000477564.1:p.Thr716= | |
ENST00000623402.1:c.2163C= | ENSP00000485276.1:p.Thr721= | |
NM_153334.6:c.2163C= | NP_699165.3:p.Thr721= | |
NM_182895.4:c.2148C= | NP_878315.2:p.Thr716= | |
NM_153334.7:c.2163C= | NP_699165.3:p.Thr721= | |
NM_182895.5:c.2148C= MANE Select | NP_878315.2:p.Thr716= |