Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169541909C= , CM000663.2:g.169541909C= | GRCh38 |
| NC_000001.10:g.169511147C= , CM000663.1:g.169511147C= | GRCh37 |
| NC_000001.9:g.167777771C= | NCBI36 |
| NG_011806.1:g.49623G= , LRG_553:g.49623G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000367797.9:c.3181G= MANE Select | ENSP00000356771.3:p.Glu1061= | |
| ENST00000367796.3:c.3196G= | ENSP00000356770.3:p.Glu1066= | |
| ENST00000367797.7:c.3181G= | ENSP00000356771.3:p.Glu1061= | |
| NM_000130.4:c.3181G= , LRG_553t1:c.3181G= | NP_000121.2:p.Glu1061= | |
| XM_017000660.2:c.2770G= | XP_016856149.1:p.Glu924= | |
| NM_000130.5:c.3181G= MANE Select | NP_000121.2:p.Glu1061= |