HGVS | Genome Assembly |
---|---|
NC_000005.10:g.134606917A= , CM000667.2:g.134606917A= | GRCh38 |
NC_000005.9:g.133942607A= , CM000667.1:g.133942607A= | GRCh37 |
NC_000005.8:g.133970506A= | NCBI36 |
NG_017002.1:g.30927T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000402673.7:c.*33T= MANE Select | ENSP00000385432.2:n.*33T= | |
ENST00000402673.6:c.*33T= | ENSP00000385432.2:n.*33T= | |
ENST00000439578.5:c.*33T= | ENSP00000404997.1:n.*33T= | |
ENST00000502539.5:c.*33T= | ENSP00000426335.1:n.*33T= | |
ENST00000507419.5:c.*33T= | ENSP00000425339.1:n.*33T= | |
ENST00000508363.5:n.2599T= | ||
NM_001033503.2:c.*33T= | NP_001028675.1:n.*33T= | |
NM_016103.3:c.*33T= | NP_057187.1:n.*33T= | |
NM_016103.4:c.*33T= MANE Select | NP_057187.1:n.*33T= | |
NM_001033503.3:c.*33T= | NP_001028675.1:n.*33T= |