Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52520005C= , CM000674.2:g.52520005C= | GRCh38 |
| NC_000012.11:g.52913789C= , CM000674.1:g.52913789C= | GRCh37 |
| NC_000012.10:g.51200056C= | NCBI36 |
| NG_008297.1:g.5455G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.292G= MANE Select | ENSP00000252242.4:p.Gly98= | |
| ENST00000252242.8:c.292G= | ENSP00000252242.4:p.Gly98= | |
| ENST00000546577.1:c.292G= | ENSP00000449651.1:p.Gly98= | |
| ENST00000549420.1:c.44-82G= | ENSP00000447209.1:n.44-82G= | |
| ENST00000551275.1:c.187G= | ENSP00000448041.1:p.Gly63= | |
| ENST00000552629.5:n.390G= | ||
| NM_000424.3:c.292G= | NP_000415.2:p.Gly98= | |
| NM_000424.4:c.292G= MANE Select | NP_000415.2:p.Gly98= |