HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31271672C= , CM000668.2:g.31271672C= | GRCh38 |
NC_000006.11:g.31239449C= , CM000668.1:g.31239449C= | GRCh37 |
NC_000006.10:g.31347428C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.270G= MANE Select | ENSP00000365402.5:p.Lys90= | |
ENST00000376228.9:c.270G= | ENSP00000365402.5:p.Lys90= | |
ENST00000376237.8:c.270G= | ENSP00000365412.4:p.Lys90= | |
ENST00000383329.7:c.270G= | ENSP00000372819.3:p.Lys90= | |
ENST00000415537.1:c.268G= | ||
ENST00000484378.1:n.289G= | ||
ENST00000487245.5:n.379G= | ||
ENST00000495835.1:n.459G= | ||
NM_002117.5:c.270G= | NP_002108.4:p.Lys90= | |
NM_002117.6:c.270G= MANE Select | NP_002108.4:p.Lys90= |