HGVS | Genome Assembly |
---|---|
NC_000006.12:g.160249250A= , CM000668.2:g.160249250A= | GRCh38 |
NC_000006.11:g.160670282A= , CM000668.1:g.160670282A= | GRCh37 |
NC_000006.10:g.160590272A= | NCBI36 |
HGVS | Amino-acid Change |
---|---|
NM_003058.4:c.808T= MANE Select | NP_003049.2:p.Ser270= |
ENST00000366953.8:c.808T= MANE Select | ENSP00000355920.3:p.Ser270= |
NM_003058.3:c.808T= | NP_003049.2:p.Ser270= |
ENST00000366952.1:c.745T= | ENSP00000355919.1:p.Ser249= |
ENST00000366953.7:c.808T= | ENSP00000355920.3:p.Ser270= |
ENST00000491092.1:n.705T= |