HGVS | Genome Assembly |
---|---|
NC_000003.12:g.150926219C= , CM000665.2:g.150926219C= | GRCh38 |
NC_000003.11:g.150644006C= , CM000665.1:g.150644006C= | GRCh37 |
NC_000003.10:g.152126696C= | NCBI36 |
NG_009168.1:g.51781G= , LRG_700:g.51781G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295911.6:c.*633G= | ENSP00000295911.2:n.*633G= | |
ENST00000562308.5:c.104+15363G= | ||
ENST00000565169.1:c.162+15363G= | ||
ENST00000569170.5:c.162+15363G= | ||
NM_052995.2:c.*633G= , LRG_700t2:c.*633G= | NP_443721.1:n.*633G= | |
XR_924167.1:n.2728G= |