Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44251257T>C , CM000679.2:g.44251257T>C | GRCh38 |
| NC_000017.10:g.42328625T>C , CM000679.1:g.42328625T>C | GRCh37 |
| NC_000017.9:g.39684151T>C | NCBI36 |
| NG_007498.1:g.21878A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262418.12:c.2557A>G MANE Select | ENSP00000262418.6:p.Thr853Ala | |
| ENST00000262418.10:c.2557A>G | ENSP00000262418.6:p.Thr853Ala | |
| ENST00000399246.3:c.1459A>G | ENSP00000382190.3:p.Thr487Ala | |
| NM_000342.3:c.2557A>G | NP_000333.1:p.Thr853Ala | |
| XM_005257593.3:c.2362A>G | XP_005257650.1:p.Thr788Ala | |
| XM_011525129.1:c.2467A>G | XP_011523431.1:p.Thr823Ala | |
| XM_005257593.5:c.2362A>G | XP_005257650.1:p.Thr788Ala | |
| XM_011525129.2:c.2467A>G | XP_011523431.1:p.Thr823Ala | |
| NM_000342.4:c.2557A>G MANE Select | NP_000333.1:p.Thr853Ala |