HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734181G= , CM000679.2:g.4734181G= | GRCh38 |
NC_000017.10:g.4637476G= , CM000679.1:g.4637476G= | GRCh37 |
NC_000017.9:g.4584225G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*322C= MANE Select | ENSP00000293778.7:n.*322C= | |
ENST00000293778.10:c.*322C= | ENSP00000293778.6:n.*322C= | |
ENST00000576153.5:n.878C= | ||
NM_022059.3:c.*322C= | NP_071342.2:n.*322C= | |
NM_022059.4:c.*322C= | NP_071342.2:n.*322C= | |
NM_001386809.1:c.*322C= MANE Select | NP_001373738.1:n.*322C= |