Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.123040605C= , CM000672.2:g.123040605C= | GRCh38 |
| NC_000010.10:g.124800121C= , CM000672.1:g.124800121C= | GRCh37 |
| NC_000010.9:g.124790111C= | NCBI36 |
| NG_008003.1:g.36693C= , LRG_451:g.36693C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001609.4:c.443C= MANE Select | NP_001600.1:p.Thr148= |
| ENST00000358776.7:c.443C= MANE Select | ENSP00000357873.3:p.Thr148= |
| NM_001330174.1:c.137C= | NP_001317103.1:p.Thr46= |
| NM_001330174.2:c.137C= | NP_001317103.1:p.Thr46= |
| NM_001330174.3:c.137C= | NP_001317103.1:p.Thr46= |
| NM_001609.3:c.443C= , LRG_451t1:c.443C= | NP_001600.1:p.Thr148= |
| ENST00000358776.6:c.443C= | ENSP00000357873.3:p.Thr148= |
| ENST00000368869.8:c.137C= | ENSP00000357862.4:p.Thr46= |
| ENST00000411816.2:n.460C= |