Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204156184C>T , CM000663.2:g.204156184C>T | GRCh38 |
| NC_000001.10:g.204125312C>T , CM000663.1:g.204125312C>T | GRCh37 |
| NC_000001.9:g.202391935C>T | NCBI36 |
| NG_012122.1:g.15154G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272190.9:c.954G>A MANE Select | ENSP00000272190.8:p.Leu318= | |
| ENST00000638118.1:c.840G>A | ENSP00000490307.1:p.Leu280= | |
| ENST00000272190.8:c.954G>A | ENSP00000272190.8:p.Leu318= | |
| NM_000537.3:c.954G>A | NP_000528.1:p.Leu318= | |
| NM_000537.4:c.954G>A MANE Select | NP_000528.1:p.Leu318= |