Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169582444T= , CM000663.2:g.169582444T= | GRCh38 |
| NC_000001.10:g.169551682T= , CM000663.1:g.169551682T= | GRCh37 |
| NC_000001.9:g.167818306T= | NCBI36 |
| NG_011806.1:g.9088A= , LRG_553:g.9088A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000130.5:c.237A= MANE Select | NP_000121.2:p.Gln79= |
| ENST00000367797.9:c.237A= MANE Select | ENSP00000356771.3:p.Gln79= |
| NM_000130.4:c.237A= , LRG_553t1:c.237A= | NP_000121.2:p.Gln79= |
| ENST00000367796.3:c.237A= | ENSP00000356770.3:p.Gln79= |
| ENST00000367797.7:c.237A= | ENSP00000356771.3:p.Gln79= |
| XM_017000660.2:c.-162+3785A= | XP_016856149.1:n.-162+3785A= |