Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.741367G>A , CM000669.2:g.741367G>A | GRCh38 |
| NC_000007.13:g.781004G>A , CM000669.1:g.781004G>A | GRCh37 |
| NC_000007.12:g.747530G>A | NCBI36 |
| NG_033137.1:g.19667G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_017802.4:c.926G>A MANE Select | NP_060272.3:p.Trp309Ter |
| ENST00000297440.11:c.926G>A MANE Select | ENSP00000297440.6:p.Trp309Ter |
| NM_017802.3:c.926G>A | NP_060272.3:p.Trp309Ter |
| NR_075098.1:n.884G>A | |
| NR_075098.2:n.886G>A | |
| ENST00000297440.10:c.926G>A | ENSP00000297440.6:p.Trp309Ter |
| ENST00000437419.5:c.243G>A | |
| ENST00000438961.1:n.395G>A | |
| ENST00000440747.5:c.330G>A | |
| XM_024446813.1:c.926G>A | XP_024302581.1:p.Trp309Ter |
| XM_024446814.1:c.320G>A | XP_024302582.1:p.Trp107Ter |