Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.123040606A>T , CM000672.2:g.123040606A>T | GRCh38 |
| NC_000010.10:g.124800122A>T , CM000672.1:g.124800122A>T | GRCh37 |
| NC_000010.9:g.124790112A>T | NCBI36 |
| NG_008003.1:g.36694A>T , LRG_451:g.36694A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358776.7:c.444A>T MANE Select | ENSP00000357873.3:p.Thr148= | |
| ENST00000358776.6:c.444A>T | ENSP00000357873.3:p.Thr148= | |
| ENST00000368869.8:c.138A>T | ENSP00000357862.4:p.Thr46= | |
| ENST00000411816.2:n.461A>T | ||
| NM_001609.3:c.444A>T , LRG_451t1:c.444A>T | NP_001600.1:p.Thr148= | |
| NM_001330174.1:c.138A>T | NP_001317103.1:p.Thr46= | |
| NM_001330174.2:c.138A>T | NP_001317103.1:p.Thr46= | |
| NM_001609.4:c.444A>T MANE Select | NP_001600.1:p.Thr148= | |
| NM_001330174.3:c.138A>T | NP_001317103.1:p.Thr46= |