HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67740647T= , CM000666.2:g.67740647T= | GRCh38 |
NC_000004.11:g.68606365T= , CM000666.1:g.68606365T= | GRCh37 |
NC_000004.10:g.68288960T= | NCBI36 |
NG_009293.1:g.20440A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226413.5:c.820A= MANE Select | ENSP00000226413.5:p.Thr274= | |
ENST00000226413.4:c.820A= | ENSP00000226413.4:p.Thr274= | |
ENST00000420975.2:c.692A= | ENSP00000397561.2:p.His231= | |
NM_000406.2:c.820A= | NP_000397.1:p.Thr274= | |
NM_001012763.1:c.692A= | NP_001012781.1:p.His231= | |
NM_000406.3:c.820A= MANE Select | NP_000397.1:p.Thr274= | |
NM_001012763.2:c.692A= | NP_001012781.1:p.His231= |