HGVS | Genome Assembly |
---|---|
NC_000006.12:g.1610707A= , CM000668.2:g.1610707A= | GRCh38 |
NC_000006.11:g.1610942A= , CM000668.1:g.1610942A= | GRCh37 |
NC_000006.10:g.1555941A= | NCBI36 |
NG_009368.1:g.5262A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000645831.2:c.262A= MANE Select | ENSP00000493906.1:p.Thr88= | |
ENST00000380874.3:c.262A= | ENSP00000370256.2:p.Thr88= | |
NM_001453.2:c.262A= | NP_001444.2:p.Thr88= | |
NM_001453.3:c.262A= MANE Select | NP_001444.2:p.Thr88= |