HGVS | Genome Assembly |
---|---|
NC_000004.12:g.71030456T= , CM000666.2:g.71030456T= | GRCh38 |
NC_000004.11:g.71896173T= , CM000666.1:g.71896173T= | GRCh37 |
NC_000004.10:g.72115037T= | NCBI36 |
NG_023303.1:g.41909T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000286648.10:c.*1078T= MANE Select | ENSP00000286648.5:n.*1078T= | |
ENST00000286648.9:c.*1078T= | ENSP00000286648.5:n.*1078T= | |
ENST00000503359.5:c.*1805T= | ENSP00000426389.1:n.*1805T= | |
ENST00000504730.5:c.*1145T= | ENSP00000425578.1:n.*1145T= | |
ENST00000504952.1:c.*1004T= | ENSP00000421508.1:n.*1004T= | |
NM_000788.2:c.*1078T= | NP_000779.1:n.*1078T= | |
NM_000788.3:c.*1078T= MANE Select | NP_000779.1:n.*1078T= |