HGVS | Genome Assembly |
---|---|
NC_000003.12:g.150926188A>T , CM000665.2:g.150926188A>T | GRCh38 |
NC_000003.11:g.150643975A>T , CM000665.1:g.150643975A>T | GRCh37 |
NC_000003.10:g.152126665A>T | NCBI36 |
NG_009168.1:g.51812T>A , LRG_700:g.51812T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295911.6:c.*664T>A | ENSP00000295911.2:n.*664T>A | |
ENST00000562308.5:c.104+15394T>A | ||
ENST00000565169.1:c.162+15394T>A | ||
ENST00000569170.5:c.162+15394T>A | ||
NM_052995.2:c.*664T>A , LRG_700t2:c.*664T>A | NP_443721.1:n.*664T>A | |
XR_924167.1:n.2759T>A |