Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153725847A>T , CM000685.2:g.153725847A>T | GRCh38 |
| NC_000023.10:g.152991302A>T , CM000685.1:g.152991302A>T | GRCh37 |
| NC_000023.9:g.152644496A>T | NCBI36 |
| NG_009022.2:g.5980A>T | |
| NG_023231.1:g.3900T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000033.4:c.581A>T MANE Select | NP_000024.2:p.Asp194Val |
| ENST00000218104.6:c.581A>T MANE Select | ENSP00000218104.3:p.Asp194Val |
| NM_000033.3:c.581A>T | NP_000024.2:p.Asp194Val |
| ENST00000218104.5:c.581A>T | ENSP00000218104.3:p.Asp194Val |
| ENST00000370129.4:c.26A>T | ENSP00000359147.3:p.Asp9Val |
| XR_938507.1:n.997A>T | |
| XR_938507.2:n.997A>T |