HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19954211A= , CM000670.2:g.19954211A= | GRCh38 |
NC_000008.10:g.19811722A= , CM000670.1:g.19811722A= | GRCh37 |
NC_000008.9:g.19856002A= | NCBI36 |
NG_008855.1:g.20141A= | |
NG_008855.2:g.57495A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650287.1:c.633A= MANE Select | ENSP00000497642.1:p.Thr211= | |
ENST00000311322.8:c.633A= | ENSP00000309757.6:p.Thr211= | |
NM_000237.2:c.633A= | NP_000228.1:p.Thr211= | |
NM_000237.3:c.633A= MANE Select | NP_000228.1:p.Thr211= |