Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48362859C= , CM000675.2:g.48362859C= | GRCh38 |
| NC_000013.10:g.48936995C= , CM000675.1:g.48936995C= | GRCh37 |
| NC_000013.9:g.47834996C= | NCBI36 |
| NG_009009.1:g.64113C= , LRG_517:g.64113C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000321.3:c.763C= MANE Select | NP_000312.2:p.Arg255= |
| ENST00000267163.6:c.763C= MANE Select | ENSP00000267163.4:p.Arg255= |
| NM_000321.2:c.763C= , LRG_517t1:c.763C= | NP_000312.2:p.Arg255= |
| ENST00000267163.4:c.763C= | ENSP00000267163.4:p.Arg255= |
| ENST00000467505.5:c.*131C= | ENSP00000434702.1:n.*131C= |
| ENST00000650461.1:c.763C= | ENSP00000497193.1:p.Arg255= |
| XM_011535171.1:c.502C= | XP_011533473.1:p.Arg168= |
| XM_011535171.2:c.502C= | XP_011533473.1:p.Arg168= |