HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31269089A= , CM000668.2:g.31269089A= | GRCh38 |
NC_000006.11:g.31236866A= , CM000668.1:g.31236866A= | GRCh37 |
NC_000006.10:g.31344845A= | NCBI36 |
NG_029422.2:g.8043T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376228.10:c.*80T= MANE Select | ENSP00000365402.5:n.*80T= | |
ENST00000376228.9:c.*80T= | ENSP00000365402.5:n.*80T= | |
ENST00000376237.8:c.*768T= | ENSP00000365412.4:n.*768T= | |
ENST00000383329.7:c.*80T= | ENSP00000372819.3:n.*80T= | |
ENST00000466892.5:n.414T= | ||
ENST00000470363.5:n.939T= | ||
ENST00000487245.5:n.1540T= | ||
NM_002117.5:c.*80T= | NP_002108.4:n.*80T= | |
NM_002117.6:c.*80T= MANE Select | NP_002108.4:n.*80T= |