Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153725304A>C , CM000685.2:g.153725304A>C | GRCh38 |
| NC_000023.10:g.152990759A>C , CM000685.1:g.152990759A>C | GRCh37 |
| NC_000023.9:g.152643953A>C | NCBI36 |
| NG_009022.2:g.5437A>C | |
| NG_023231.1:g.4443T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218104.6:c.38A>C MANE Select | ENSP00000218104.3:p.Asn13Thr | |
| ENST00000218104.5:c.38A>C | ENSP00000218104.3:p.Asn13Thr | |
| NM_000033.3:c.38A>C | NP_000024.2:p.Asn13Thr | |
| XR_938507.1:n.454A>C | ||
| XR_938507.2:n.454A>C | ||
| NM_000033.4:c.38A>C MANE Select | NP_000024.2:p.Asn13Thr |