HGVS | Genome Assembly |
---|---|
NC_000014.9:g.36663370T= , CM000676.2:g.36663370T= | GRCh38 |
NC_000014.8:g.37132575T= , CM000676.1:g.37132575T= | GRCh37 |
NC_000014.7:g.36202326T= | NCBI36 |
NG_013357.1:g.10803T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000361487.7:c.478T= MANE Select | ENSP00000355245.6:p.Tyr160= | |
ENST00000361487.6:c.478T= | ENSP00000355245.6:p.Tyr160= | |
ENST00000402703.6:c.478T= | ENSP00000384817.2:p.Tyr160= | |
ENST00000554201.1:c.-84T= | ENSP00000450434.1:n.-84T= | |
NM_006194.3:c.478T= | NP_006185.1:p.Tyr160= | |
NM_001372076.1:c.478T= MANE Select | NP_001359005.1:p.Tyr160= | |
NM_006194.4:c.478T= | NP_006185.1:p.Tyr160= |