Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.46003487G= , CM000683.2:g.46003487G= | GRCh38 |
| NC_000021.8:g.47423401G= , CM000683.1:g.47423401G= | GRCh37 |
| NC_000021.7:g.46247829G= | NCBI36 |
| NG_008674.1:g.26739G= , LRG_475:g.26739G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000463060.6:n.960G= | ||
| ENST00000612273.2:c.687G= | ||
| ENST00000682634.1:c.687G= | ||
| ENST00000361866.8:c.2561G= MANE Select | ENSP00000355180.3:p.Arg854= | |
| ENST00000361866.7:c.2561G= | ENSP00000355180.3:p.Arg854= | |
| ENST00000486023.1:n.349G= | ||
| ENST00000498614.5:n.795G= | ||
| ENST00000612273.1:c.2555G= | ENSP00000483630.1:p.Arg852= | |
| NM_001848.2:c.2561G= , LRG_475t1:c.2561G= | NP_001839.2:p.Arg854= | |
| NM_001848.3:c.2561G= MANE Select | NP_001839.2:p.Arg854= |