HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734422T= , CM000679.2:g.4734422T= | GRCh38 |
NC_000017.10:g.4637717T= , CM000679.1:g.4637717T= | GRCh37 |
NC_000017.9:g.4584466T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*81A= MANE Select | ENSP00000293778.7:n.*81A= | |
ENST00000574412.6:c.*184A= | ENSP00000459592.2:n.*184A= | |
ENST00000293778.10:c.*81A= | ENSP00000293778.6:n.*81A= | |
ENST00000574412.5:c.*184A= | ENSP00000459592.1:n.*184A= | |
ENST00000576153.5:n.637A= | ||
NM_022059.3:c.*81A= | NP_071342.2:n.*81A= | |
NM_022059.4:c.*81A= | NP_071342.2:n.*81A= | |
NM_001386809.1:c.*81A= MANE Select | NP_001373738.1:n.*81A= |