Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.127854342G= , CM000671.2:g.127854342G= | GRCh38 |
| NC_000009.11:g.130616621G= , CM000671.1:g.130616621G= | GRCh37 |
| NC_000009.10:g.129656442G= | NCBI36 |
| NG_009551.1:g.5427C= , LRG_589:g.5427C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001114753.3:c.14C= MANE Select | NP_001108225.1:p.Thr5= |
| ENST00000373203.9:c.14C= MANE Select | ENSP00000362299.4:p.Thr5= |
| NM_000118.3:c.14C= , LRG_589t1:c.14C= | NP_000109.1:p.Thr5= |
| NM_001114753.2:c.14C= , LRG_589t2:c.14C= | NP_001108225.1:p.Thr5= |
| ENST00000344849.4:c.14C= | ENSP00000341917.3:p.Thr5= |
| ENST00000373203.8:c.14C= | ENSP00000362299.4:p.Thr5= |