Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12718165T>G , CM000674.2:g.12718165T>G | GRCh38 |
| NC_000012.11:g.12871099T>G , CM000674.1:g.12871099T>G | GRCh37 |
| NC_000012.10:g.12762366T>G | NCBI36 |
| NG_016341.1:g.5798T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004064.5:c.326T>G MANE Select | NP_004055.1:p.Val109Gly |
| ENST00000228872.9:c.326T>G MANE Select | ENSP00000228872.4:p.Val109Gly |
| NM_004064.4:c.326T>G | NP_004055.1:p.Val109Gly |
| ENST00000228872.8:c.326T>G | ENSP00000228872.4:p.Val109Gly |
| ENST00000396340.1:c.326T>G | ENSP00000379629.1:p.Val109Gly |
| ENST00000442489.1:c.193+112T>G | ENSP00000407597.1:n.193+112T>G |
| ENST00000477087.1:n.155-660T>G | |
| ENST00000614874.2:c.326T>G | ENSP00000507272.1:p.Val109Gly |
| ENST00000682620.1:n.1631-660T>G | |
| ENST00000684771.1:n.585-660T>G |