Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.72376091C= , CM000677.2:g.72376091C= | GRCh38 |
| NC_000015.9:g.72668432C= , CM000677.1:g.72668432C= | GRCh37 |
| NC_000015.8:g.70455486C= | NCBI36 |
| NG_009017.1:g.5089G= | |
| NG_009017.2:g.5089G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268097.9:c.-119G= | ENSP00000268097.5:n.-119G= | |
| ENST00000569509.5:n.146+184G= | ||
| NM_000520.4:c.-119G= | NP_000511.2:n.-119G= | |
| NM_000520.5:c.-119G= | NP_000511.2:n.-119G= | |
| NM_001318825.1:c.-119G= | NP_001305754.1:n.-119G= | |
| NR_134869.1:n.383G= |