Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.81354478C= , CM000678.2:g.81354478C= | GRCh38 |
| NC_000016.9:g.81388083C= , CM000678.1:g.81388083C= | GRCh37 |
| NC_000016.8:g.79945584C= | NCBI36 |
| NG_009007.1:g.44513C= , LRG_242:g.44513C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648349.2:c.*64C= | ENSP00000498114.1:n.*64C= | |
| ENST00000648994.2:c.356C= MANE Select | ENSP00000497351.1:p.Thr119= | |
| ENST00000650388.1:c.168-2307C= | ENSP00000498081.1:n.168-2307C= | |
| ENST00000674788.1:n.481C= | ||
| ENST00000568107.2:c.356C= | ENSP00000476795.1:p.Thr119= | |
| NM_022041.3:c.356C= , LRG_242t1:c.356C= | NP_071324.1:p.Thr119= | |
| XM_017023734.1:c.-284C= | XP_016879223.1:n.-284C= | |
| NM_001377486.1:c.-284C= | NP_001364415.1:n.-284C= | |
| NM_022041.4:c.356C= MANE Select | NP_071324.1:p.Thr119= |