Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169552704G= , CM000663.2:g.169552704G= | GRCh38 |
| NC_000001.10:g.169521942G= , CM000663.1:g.169521942G= | GRCh37 |
| NC_000001.9:g.167788566G= | NCBI36 |
| NG_011806.1:g.38828C= , LRG_553:g.38828C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367797.9:c.1149C= MANE Select | ENSP00000356771.3:p.Phe383= | |
| ENST00000367796.3:c.1149C= | ENSP00000356770.3:p.Phe383= | |
| ENST00000367797.7:c.1149C= | ENSP00000356771.3:p.Phe383= | |
| NM_000130.4:c.1149C= , LRG_553t1:c.1149C= | NP_000121.2:p.Phe383= | |
| XM_017000660.2:c.738C= | XP_016856149.1:p.Phe246= | |
| NM_000130.5:c.1149C= MANE Select | NP_000121.2:p.Phe383= |