Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45992022G= , CM000683.2:g.45992022G= | GRCh38 |
| NC_000021.8:g.47411936G= , CM000683.1:g.47411936G= | GRCh37 |
| NC_000021.7:g.46236364G= | NCBI36 |
| NG_008674.1:g.15274G= , LRG_475:g.15274G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001848.3:c.1132G= MANE Select | NP_001839.2:p.Ala378= |
| ENST00000361866.8:c.1132G= MANE Select | ENSP00000355180.3:p.Ala378= |
| NM_001848.2:c.1132G= , LRG_475t1:c.1132G= | NP_001839.2:p.Ala378= |
| ENST00000361866.7:c.1132G= | ENSP00000355180.3:p.Ala378= |
| ENST00000612273.1:c.1132G= | ENSP00000483630.1:p.Ala378= |