Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229431874G= , CM000663.2:g.229431874G= | GRCh38 |
| NC_000001.10:g.229567621G= , CM000663.1:g.229567621G= | GRCh37 |
| NC_000001.9:g.227634244G= | NCBI36 |
| NG_006672.1:g.7223C= , LRG_429:g.7223C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366683.4:c.837C= | ENSP00000355644.4:p.Thr279= | |
| ENST00000684723.1:c.702C= | ENSP00000508084.1:p.Thr234= | |
| ENST00000366683.3:c.480-12C= | ENSP00000355644.3:n.480-12C= | |
| ENST00000366684.7:c.837C= MANE Select | ENSP00000355645.3:p.Thr279= | |
| NM_001100.3:c.837C= , LRG_429t1:c.837C= | NP_001091.1:p.Thr279= | |
| NM_001100.4:c.837C= MANE Select | NP_001091.1:p.Thr279= |