Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2278337C= , CM000678.2:g.2278337C= | GRCh38 |
| NC_000016.9:g.2328338C= , CM000678.1:g.2328338C= | GRCh37 |
| NC_000016.8:g.2268339C= | NCBI36 |
| NG_011790.1:g.67410G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301732.10:c.4669G= MANE Select | ENSP00000301732.5:p.Val1557= | |
| ENST00000301732.9:c.4669G= | ENSP00000301732.5:p.Val1557= | |
| ENST00000382381.7:c.4495G= | ENSP00000371818.3:p.Val1499= | |
| ENST00000566200.1:n.1190G= | ||
| NM_001089.2:c.4669G= | NP_001080.2:p.Val1557= | |
| NM_001089.3:c.4669G= MANE Select | NP_001080.2:p.Val1557= |