Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8120721C= , CM000679.2:g.8120721C= | GRCh38 |
| NC_000017.10:g.8024039C= , CM000679.1:g.8024039C= | GRCh37 |
| NC_000017.9:g.7964764C= | NCBI36 |
| NG_015807.1:g.3196G= | |
| NG_015816.1:g.8372G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000541682.7:c.*850G= MANE Select | ENSP00000446205.2:n.*850G= | |
| ENST00000541682.6:c.1543G= | ENSP00000446205.2:n.1543G= | |
| NM_001165967.1:c.*850G= | NP_001159439.1:n.*850G= | |
| NM_032580.3:c.*850G= | NP_115969.2:n.*850G= | |
| XM_011524038.1:c.*850G= | XP_011522340.1:n.*850G= | |
| XR_934203.1:n.69+907C= | ||
| XM_017025232.1:c.*850G= | XP_016880721.1:n.*850G= | |
| XM_024451007.1:c.*850G= | XP_024306775.1:n.*850G= | |
| NM_001165967.2:c.*850G= MANE Select | NP_001159439.1:n.*850G= | |
| NM_032580.4:c.*850G= | NP_115969.2:n.*850G= |