Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.97598859C= , CM000672.2:g.97598859C= | GRCh38 |
| NC_000010.10:g.99358616C= , CM000672.1:g.99358616C= | GRCh37 |
| NC_000010.9:g.99348606C= | NCBI36 |
| NG_027922.1:g.19515C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000370646.9:c.296C= MANE Select | ENSP00000359680.4:p.Ala99= | |
| ENST00000370646.8:c.296C= | ENSP00000359680.4:p.Ala99= | |
| ENST00000370647.8:c.212-2998C= | ENSP00000359681.4:n.212-2998C= | |
| ENST00000370649.3:c.212-2998C= | ENSP00000359683.3:n.212-2998C= | |
| ENST00000465608.1:n.677C= | ||
| NM_001134670.1:c.212-2998C= | NP_001128142.1:n.212-2998C= | |
| NM_138413.3:c.296C= | NP_612422.2:p.Ala99= | |
| NM_138413.4:c.296C= MANE Select | NP_612422.2:p.Ala99= | |
| NM_001134670.2:c.212-2998C= | NP_001128142.1:n.212-2998C= |