Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57763692T= , CM000674.2:g.57763692T= | GRCh38 |
| NC_000012.11:g.58157475T= , CM000674.1:g.58157475T= | GRCh37 |
| NC_000012.10:g.56443742T= | NCBI36 |
| NG_007076.1:g.8502A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000713544.1:c.1413A= | ENSP00000518840.1:p.Ala471= | |
| ENST00000713545.1:c.*337A= | ENSP00000518841.1:n.*337A= | |
| ENST00000228606.9:c.1332A= MANE Select | ENSP00000228606.4:p.Ala444= | |
| ENST00000228606.8:c.1332A= | ENSP00000228606.4:p.Ala444= | |
| ENST00000547344.5:n.1471A= | ||
| NM_000785.3:c.1332A= | NP_000776.1:p.Ala444= | |
| NM_000785.4:c.1332A= MANE Select | NP_000776.1:p.Ala444= |