Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8745677G= , CM000665.2:g.8745677G= | GRCh38 |
| NC_000003.11:g.8787363G= , CM000665.1:g.8787363G= | GRCh37 |
| NC_000003.10:g.8762363G= | NCBI36 |
| NG_008797.2:g.16868G= , LRG_329:g.16868G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000343849.3:c.266G= MANE Select | ENSP00000341940.2:p.Gly89= | |
| ENST00000343849.2:c.266G= | ENSP00000341940.2:p.Gly89= | |
| ENST00000397368.2:c.266G= | ENSP00000380525.2:p.Gly89= | |
| ENST00000472766.1:n.155+11687G= | ||
| NM_001234.4:c.266G= | NP_001225.1:p.Gly89= | |
| NM_033337.2:c.266G= , LRG_329t1:c.266G= | NP_203123.1:p.Gly89= | |
| NM_001234.5:c.266G= | NP_001225.1:p.Gly89= | |
| NM_033337.3:c.266G= MANE Select | NP_203123.1:p.Gly89= |