Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.150926367C= , CM000665.2:g.150926367C= | GRCh38 |
| NC_000003.11:g.150644154C= , CM000665.1:g.150644154C= | GRCh37 |
| NC_000003.10:g.152126844C= | NCBI36 |
| NG_009168.1:g.51633G= , LRG_700:g.51633G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295911.6:c.*485G= | ENSP00000295911.2:n.*485G= | |
| ENST00000562308.5:c.104+15215G= | ||
| ENST00000565169.1:c.162+15215G= | ||
| ENST00000569170.5:c.162+15215G= | ||
| NM_052995.2:c.*485G= , LRG_700t2:c.*485G= | NP_443721.1:n.*485G= | |
| XR_924167.1:n.2580G= |