Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.139537158A= , CM000685.2:g.139537158A= | GRCh38 |
| NC_000023.10:g.138619317A= , CM000685.1:g.138619317A= | GRCh37 |
| NC_000023.9:g.138446983A= | NCBI36 |
| NG_007994.1:g.11423A= , LRG_556:g.11423A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218099.7:c.237A= MANE Select | ENSP00000218099.2:p.Glu79= | |
| ENST00000218099.6:c.237A= | ENSP00000218099.2:p.Glu79= | |
| ENST00000394090.2:c.237A= | ENSP00000377650.2:p.Glu79= | |
| ENST00000479617.2:n.241+3A= | ||
| NM_000133.3:c.237A= , LRG_556t1:c.237A= | NP_000124.1:p.Glu79= | |
| NM_001313913.1:c.237A= | NP_001300842.1:p.Glu79= | |
| XM_005262397.3:c.237A= | XP_005262454.1:p.Glu79= | |
| XM_005262397.4:c.237A= | XP_005262454.1:p.Glu79= | |
| NM_000133.4:c.237A= MANE Select | NP_000124.1:p.Glu79= | |
| NM_001313913.2:c.237A= | NP_001300842.1:p.Glu79= |