Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133353757G>A , CM000671.2:g.133353757G>A | GRCh38 |
| NC_000009.10:g.135210433G>A | NCBI36 |
| NG_008477.1:g.7750C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003172.4:c.507C>T MANE Select | NP_003163.1:p.Thr169= |
| ENST00000371974.8:c.507C>T MANE Select | ENSP00000361042.3:p.Thr169= |
| NM_001280787.1:c.180C>T | NP_001267716.1:p.Thr60= |
| NM_003172.3:c.507C>T | NP_003163.1:p.Thr169= |
| ENST00000371974.7:c.507C>T | ENSP00000361042.3:p.Thr169= |
| ENST00000437995.1:n.453C>T | |
| ENST00000495952.5:n.497C>T | |
| ENST00000615505.4:c.180C>T | ENSP00000482067.1:p.Thr60= |
| XM_011518942.1:c.180C>T | XP_011517244.1:p.Thr60= |