Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153725709A= , CM000685.2:g.153725709A= | GRCh38 |
| NC_000023.10:g.152991164A= , CM000685.1:g.152991164A= | GRCh37 |
| NC_000023.9:g.152644358A= | NCBI36 |
| NG_009022.2:g.5842A= | |
| NG_023231.1:g.4038T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218104.6:c.443A= MANE Select | ENSP00000218104.3:p.Asn148= | |
| ENST00000218104.5:c.443A= | ENSP00000218104.3:p.Asn148= | |
| NM_000033.3:c.443A= | NP_000024.2:p.Asn148= | |
| XR_938507.1:n.859A= | ||
| XR_938507.2:n.859A= | ||
| NM_000033.4:c.443A= MANE Select | NP_000024.2:p.Asn148= |