Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52520263C= , CM000674.2:g.52520263C= | GRCh38 |
| NC_000012.11:g.52914047C= , CM000674.1:g.52914047C= | GRCh37 |
| NC_000012.10:g.51200314C= | NCBI36 |
| NG_008297.1:g.5197G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.34G= MANE Select | ENSP00000252242.4:p.Gly12= | |
| ENST00000252242.8:c.34G= | ENSP00000252242.4:p.Gly12= | |
| ENST00000546577.1:c.34G= | ENSP00000449651.1:p.Gly12= | |
| ENST00000549420.1:c.34G= | ENSP00000447209.1:p.Gly12= | |
| ENST00000551275.1:c.34G= | ENSP00000448041.1:p.Gly12= | |
| ENST00000552629.5:n.132G= | ||
| NM_000424.3:c.34G= | NP_000415.2:p.Gly12= | |
| NM_000424.4:c.34G= MANE Select | NP_000415.2:p.Gly12= |