Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.1250169C= , CM000673.2:g.1250169C= | GRCh38 |
| NC_000011.9:g.1271399C= , CM000673.1:g.1271399C= | GRCh37 |
| NC_000011.8:g.1227975C= | NCBI36 |
| NG_031880.1:g.32105C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002458.3:c.13289C= MANE Select | NP_002449.2:p.Thr4430= |
| ENST00000529681.5:c.13289C= MANE Select | ENSP00000436812.1:p.Thr4430= |
| NM_002458.2:c.13289C= | NP_002449.2:p.Thr4430= |