HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734418A= , CM000679.2:g.4734418A= | GRCh38 |
NC_000017.10:g.4637713A= , CM000679.1:g.4637713A= | GRCh37 |
NC_000017.9:g.4584462A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*85T= MANE Select | ENSP00000293778.7:n.*85T= | |
ENST00000574412.6:c.*188T= | ENSP00000459592.2:n.*188T= | |
ENST00000293778.10:c.*85T= | ENSP00000293778.6:n.*85T= | |
ENST00000574412.5:c.*188T= | ENSP00000459592.1:n.*188T= | |
ENST00000576153.5:n.641T= | ||
NM_022059.3:c.*85T= | NP_071342.2:n.*85T= | |
NM_022059.4:c.*85T= | NP_071342.2:n.*85T= | |
NM_001386809.1:c.*85T= MANE Select | NP_001373738.1:n.*85T= |