Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169541826A>T , CM000663.2:g.169541826A>T | GRCh38 |
| NC_000001.10:g.169511064A>T , CM000663.1:g.169511064A>T | GRCh37 |
| NC_000001.9:g.167777688A>T | NCBI36 |
| NG_011806.1:g.49706T>A , LRG_553:g.49706T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367797.9:c.3264T>A MANE Select | ENSP00000356771.3:p.Ser1088= | |
| ENST00000367796.3:c.3279T>A | ENSP00000356770.3:p.Ser1093= | |
| ENST00000367797.7:c.3264T>A | ENSP00000356771.3:p.Ser1088= | |
| NM_000130.4:c.3264T>A , LRG_553t1:c.3264T>A | NP_000121.2:p.Ser1088= | |
| XM_017000660.2:c.2853T>A | XP_016856149.1:p.Ser951= | |
| NM_000130.5:c.3264T>A MANE Select | NP_000121.2:p.Ser1088= |