Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.81365254G= , CM000678.2:g.81365254G= | GRCh38 |
| NC_000016.9:g.81398859G= , CM000678.1:g.81398859G= | GRCh37 |
| NC_000016.8:g.79956360G= | NCBI36 |
| NG_009007.1:g.55289G= , LRG_242:g.55289G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648349.2:c.*1082-96G= | ENSP00000498114.1:n.*1082-96G= | |
| ENST00000648994.2:c.1374-96G= MANE Select | ENSP00000497351.1:n.1374-96G= | |
| ENST00000650388.1:c.908-96G= | ENSP00000498081.1:n.908-96G= | |
| ENST00000568107.2:c.1374-96G= | ENSP00000476795.1:n.1374-96G= | |
| NM_022041.3:c.1374-96G= , LRG_242t1:c.1374-96G= | NP_071324.1:n.1374-96G= | |
| XM_017023734.1:c.735-96G= | XP_016879223.1:n.735-96G= | |
| NM_001377486.1:c.735-96G= | NP_001364415.1:n.735-96G= | |
| NM_022041.4:c.1374-96G= MANE Select | NP_071324.1:n.1374-96G= |