HGVS | Genome Assembly |
---|---|
NC_000016.10:g.82148415A= , CM000678.2:g.82148415A= | GRCh38 |
NC_000016.9:g.82182020A= , CM000678.1:g.82182020A= | GRCh37 |
NC_000016.8:g.80739521A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258169.9:c.*316T= MANE Select | ENSP00000258169.4:n.*316T= | |
ENST00000258169.8:c.*316T= | ENSP00000258169.4:n.*316T= | |
ENST00000563100.5:c.*72+244T= | ENSP00000454996.1:n.*72+244T= | |
NM_005792.2:c.*316T= MANE Select | NP_005783.2:n.*316T= | |
XM_011522808.1:c.*316T= | XP_011521110.1:n.*316T= | |
XM_011522808.3:c.*316T= | XP_011521110.1:n.*316T= |