HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734192C= , CM000679.2:g.4734192C= | GRCh38 |
NC_000017.10:g.4637487C= , CM000679.1:g.4637487C= | GRCh37 |
NC_000017.9:g.4584236C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*311G= MANE Select | ENSP00000293778.7:n.*311G= | |
ENST00000293778.10:c.*311G= | ENSP00000293778.6:n.*311G= | |
ENST00000576153.5:n.867G= | ||
NM_022059.3:c.*311G= | NP_071342.2:n.*311G= | |
NM_022059.4:c.*311G= | NP_071342.2:n.*311G= | |
NM_001386809.1:c.*311G= MANE Select | NP_001373738.1:n.*311G= |