Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55482069G= , CM000681.2:g.55482069G= | GRCh38 |
| NC_000019.9:g.55993436G= , CM000681.1:g.55993436G= | GRCh37 |
| NC_000019.8:g.60685248G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_033113.3:c.876G= MANE Select | NP_149104.3:p.Glu292= |
| ENST00000598519.2:c.876G= MANE Select | ENSP00000469591.1:p.Glu292= |
| NM_033113.2:c.876G= | NP_149104.3:p.Glu292= |
| ENST00000391718.3:c.873G= | ENSP00000375598.3:p.Glu291= |
| ENST00000598519.1:c.876G= | ENSP00000469591.1:p.Glu292= |
| XM_005259371.2:c.864G= | XP_005259428.1:p.Glu288= |
| XM_005259371.3:c.864G= | XP_005259428.1:p.Glu288= |
| XM_024451752.1:c.876G= | XP_024307520.1:p.Glu292= |