Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4368914T= , CM000674.2:g.4368914T= | GRCh38 |
| NC_000012.11:g.4478080T= , CM000674.1:g.4478080T= | GRCh37 |
| NC_000012.10:g.4348341T= | NCBI36 |
| NG_007087.1:g.15815A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_020638.3:c.*1429A= MANE Select | NP_065689.1:n.*1429A= |
| ENST00000237837.2:c.*1429A= MANE Select | ENSP00000237837.1:n.*1429A= |
| NM_020638.2:c.*1429A= | NP_065689.1:n.*1429A= |
| ENST00000237837.1:c.*1429A= | ENSP00000237837.1:n.*1429A= |
| ENST00000648100.1:c.*1967+2632T= | ENSP00000497536.1:n.*1967+2632T= |
| ENST00000674624.1:c.*1204+2632T= | ENSP00000501898.1:n.*1204+2632T= |