Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.97598784T>C , CM000672.2:g.97598784T>C | GRCh38 |
| NC_000010.10:g.99358541T>C , CM000672.1:g.99358541T>C | GRCh37 |
| NC_000010.9:g.99348531T>C | NCBI36 |
| NG_027922.1:g.19440T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_138413.4:c.221T>C MANE Select | NP_612422.2:p.Val74Ala |
| ENST00000370646.9:c.221T>C MANE Select | ENSP00000359680.4:p.Val74Ala |
| NM_001134670.1:c.212-3073T>C | NP_001128142.1:n.212-3073T>C |
| NM_001134670.2:c.212-3073T>C | NP_001128142.1:n.212-3073T>C |
| NM_138413.3:c.221T>C | NP_612422.2:p.Val74Ala |
| ENST00000370646.8:c.221T>C | ENSP00000359680.4:p.Val74Ala |
| ENST00000370647.8:c.212-3073T>C | ENSP00000359681.4:n.212-3073T>C |
| ENST00000370649.3:c.212-3073T>C | ENSP00000359683.3:n.212-3073T>C |
| ENST00000465608.1:n.602T>C |