HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31268963A= , CM000668.2:g.31268963A= | GRCh38 |
NC_000006.11:g.31236740A= , CM000668.1:g.31236740A= | GRCh37 |
NC_000006.10:g.31344719A= | NCBI36 |
NG_029422.2:g.8169T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.*206T= MANE Select | ENSP00000365402.5:n.*206T= | |
ENST00000376228.9:c.*206T= | ENSP00000365402.5:n.*206T= | |
ENST00000376237.8:c.*894T= | ENSP00000365412.4:n.*894T= | |
ENST00000383329.7:c.*206T= | ENSP00000372819.3:n.*206T= | |
ENST00000466892.5:n.540T= | ||
ENST00000470363.5:n.1065T= | ||
ENST00000487245.5:n.1666T= | ||
NM_002117.5:c.*206T= | NP_002108.4:n.*206T= | |
NM_002117.6:c.*206T= MANE Select | NP_002108.4:n.*206T= |