Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57766119C= , CM000674.2:g.57766119C= | GRCh38 |
| NC_000012.11:g.58159902C= , CM000674.1:g.58159902C= | GRCh37 |
| NC_000012.10:g.56446169C= | NCBI36 |
| NG_007076.1:g.6075G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000546609.2:n.186G= | ||
| ENST00000713544.1:c.274G= | ENSP00000518840.1:p.Ala92= | |
| ENST00000713545.1:c.274G= | ENSP00000518841.1:p.Ala92= | |
| ENST00000228606.9:c.274G= MANE Select | ENSP00000228606.4:p.Ala92= | |
| ENST00000228606.8:c.274G= | ENSP00000228606.4:p.Ala92= | |
| ENST00000546496.1:n.102G= | ||
| ENST00000546609.1:c.186G= | ||
| ENST00000547344.5:n.328G= | ||
| ENST00000552186.1:n.393G= | ||
| NM_000785.3:c.274G= | NP_000776.1:p.Ala92= | |
| NM_000785.4:c.274G= MANE Select | NP_000776.1:p.Ala92= |