Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110178130T>C , CM000675.2:g.110178130T>C | GRCh38 |
| NC_000013.10:g.110830477T>C , CM000675.1:g.110830477T>C | GRCh37 |
| NC_000013.9:g.109628478T>C | NCBI36 |
| NG_011544.2:g.134020A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001845.6:c.2560A>G MANE Select | NP_001836.3:p.Thr854Ala |
| ENST00000375820.10:c.2560A>G MANE Select | ENSP00000364979.4:p.Thr854Ala |
| NM_001845.5:c.2560A>G | NP_001836.3:p.Thr854Ala |
| ENST00000375820.8:c.2560A>G | ENSP00000364979.4:p.Thr854Ala |
| XM_011521048.1:c.2368A>G | XP_011519350.1:p.Thr790Ala |
| XM_011521048.2:c.2368A>G | XP_011519350.1:p.Thr790Ala |