Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42909410T= , CM000679.2:g.42909410T= | GRCh38 |
| NC_000017.10:g.41061427T= , CM000679.1:g.41061427T= | GRCh37 |
| NC_000017.9:g.38314953T= | NCBI36 |
| NG_011808.1:g.13613T= , LRG_147:g.13613T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253801.7:c.554T= MANE Select | ENSP00000253801.1:p.Val185= | |
| ENST00000253801.6:c.554T= | ENSP00000253801.1:p.Val185= | |
| ENST00000585489.1:c.447-1505T= | ENSP00000466202.1:n.447-1505T= | |
| ENST00000592383.5:c.477T= | ENSP00000465958.1:p.Ser159= | |
| NM_000151.3:c.554T= | NP_000142.2:p.Val185= | |
| NM_001270397.1:c.477T= | NP_001257326.1:p.Ser159= | |
| NM_000151.4:c.554T= MANE Select | NP_000142.2:p.Val185= | |
| NM_001270397.2:c.477T= | NP_001257326.1:p.Ser159= |