HGVS | Genome Assembly |
---|---|
NC_000003.12:g.150926231A= , CM000665.2:g.150926231A= | GRCh38 |
NC_000003.11:g.150644018A= , CM000665.1:g.150644018A= | GRCh37 |
NC_000003.10:g.152126708A= | NCBI36 |
NG_009168.1:g.51769T= , LRG_700:g.51769T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295911.6:c.*621T= | ENSP00000295911.2:n.*621T= | |
ENST00000562308.5:c.104+15351T= | ||
ENST00000565169.1:c.162+15351T= | ||
ENST00000569170.5:c.162+15351T= | ||
NM_052995.2:c.*621T= , LRG_700t2:c.*621T= | NP_443721.1:n.*621T= | |
XR_924167.1:n.2716T= |