Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.128945638C= , CM000671.2:g.128945638C= | GRCh38 |
| NC_000009.11:g.131707917C= , CM000671.1:g.131707917C= | GRCh37 |
| NC_000009.10:g.130747738C= | NCBI36 |
| NG_017009.1:g.7096G= , LRG_744:g.7096G= | |
| NG_033111.1:g.2946C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372586.4:c.*49G= MANE Select | ENSP00000361667.3:n.*49G= | |
| ENST00000372586.3:c.*49G= | ENSP00000361667.3:n.*49G= | |
| ENST00000482796.1:c.39-3551C= | ENSP00000417556.2:n.39-3551C= | |
| NM_014908.3:c.*49G= , LRG_744t1:c.*49G= | NP_055723.1:n.*49G= | |
| NM_014908.4:c.*49G= MANE Select | NP_055723.1:n.*49G= |