Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31595154A>G , CM000680.2:g.31595154A>G | GRCh38 |
| NC_000018.9:g.29175117A>G , CM000680.1:g.29175117A>G | GRCh37 |
| NC_000018.8:g.27429115A>G | NCBI36 |
| NG_009490.1:g.8388A>G , LRG_416:g.8388A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000371.4:c.235A>G MANE Select | NP_000362.1:p.Thr79Ala |
| ENST00000237014.8:c.235A>G MANE Select | ENSP00000237014.4:p.Thr79Ala |
| NM_000371.3:c.235A>G , LRG_416t1:c.235A>G | NP_000362.1:p.Thr79Ala |
| ENST00000237014.7:c.235A>G | ENSP00000237014.3:p.Thr79Ala |
| ENST00000541025.2:n.261A>G | |
| ENST00000610404.4:c.235A>G | ENSP00000477599.1:p.Thr79Ala |
| ENST00000610404.5:c.139A>G | ENSP00000477599.2:p.Thr47Ala |
| ENST00000613781.1:c.235A>G | ENSP00000479174.1:p.Thr79Ala |
| ENST00000649620.1:c.235A>G | ENSP00000497927.1:p.Thr79Ala |