Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52519029C= , CM000674.2:g.52519029C= | GRCh38 |
| NC_000012.11:g.52912813C= , CM000674.1:g.52912813C= | GRCh37 |
| NC_000012.10:g.51199080C= | NCBI36 |
| NG_008297.1:g.6431G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.687G= MANE Select | ENSP00000252242.4:p.Gln229= | |
| ENST00000252242.8:c.687G= | ENSP00000252242.4:p.Gln229= | |
| ENST00000549420.1:c.357G= | ENSP00000447209.1:p.Gln119= | |
| ENST00000551013.1:n.215G= | ||
| ENST00000551188.5:c.89G= | ||
| ENST00000552629.5:n.785G= | ||
| NM_000424.3:c.687G= | NP_000415.2:p.Gln229= | |
| NM_000424.4:c.687G= MANE Select | NP_000415.2:p.Gln229= |