Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.109087599C= , CM000670.2:g.109087599C= | GRCh38 |
| NC_000008.10:g.110099828C= , CM000670.1:g.110099828C= | GRCh37 |
| NC_000008.9:g.110169004C= | NCBI36 |
| NG_017161.1:g.5153C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000518632.2:c.87C= MANE Select | ENSP00000430711.2:p.Ile29= | |
| ENST00000311762.2:c.87C= | ENSP00000309818.2:p.Ile29= | |
| ENST00000518632.1:c.87C= | ENSP00000430711.1:p.Ile29= | |
| NM_003301.5:c.87C= | NP_003292.1:p.Ile29= | |
| XM_011517263.1:c.87C= | XP_011515565.1:p.Ile29= | |
| XM_011517263.2:c.87C= | XP_011515565.1:p.Ile29= | |
| NM_003301.7:c.87C= MANE Select | NP_003292.1:p.Ile29= |