Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.80275074G= , CM000672.2:g.80275074G= | GRCh38 |
| NC_000010.10:g.82034830G= , CM000672.1:g.82034830G= | GRCh37 |
| NC_000010.9:g.82024810G= | NCBI36 |
| NG_008083.1:g.19605C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372213.8:c.894C= MANE Select | ENSP00000361287.3:p.Ala298= | |
| ENST00000372213.7:c.894C= | ENSP00000361287.3:p.Ala298= | |
| ENST00000480845.1:n.126C= | ||
| ENST00000485270.5:n.406C= | ||
| NM_000429.2:c.894C= | NP_000420.1:p.Ala298= | |
| XM_005269842.3:c.894C= | XP_005269899.1:p.Ala298= | |
| XM_005269843.3:c.771C= | XP_005269900.1:p.Ala257= | |
| NM_000429.3:c.894C= MANE Select | NP_000420.1:p.Ala298= |