Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86575860C= , CM000670.2:g.86575860C= | GRCh38 |
| NC_000008.10:g.87588088C= , CM000670.1:g.87588088C= | GRCh37 |
| NC_000008.9:g.87657204C= | NCBI36 |
| NG_016980.1:g.172816G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.2374G= MANE Select | ENSP00000316605.5:p.Ala792= | |
| ENST00000681546.1:n.2194G= | ||
| ENST00000681746.1:c.*785G= | ENSP00000505959.1:n.*785G= | |
| ENST00000320005.5:c.2374G= | ENSP00000316605.5:p.Ala792= | |
| ENST00000517327.5:c.276+2829G= | ENSP00000428329.1:n.276+2829G= | |
| NM_019098.4:c.2374G= | NP_061971.3:p.Ala792= | |
| XM_011517138.1:c.1960G= | XP_011515440.1:p.Ala654= | |
| XM_011517138.2:c.1960G= | XP_011515440.1:p.Ala654= | |
| NM_019098.5:c.2374G= MANE Select | NP_061971.3:p.Ala792= |