Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45990419G>T , CM000683.2:g.45990419G>T | GRCh38 |
| NC_000021.8:g.47410333G>T , CM000683.1:g.47410333G>T | GRCh37 |
| NC_000021.7:g.46234761G>T | NCBI36 |
| NG_008674.1:g.13671G>T , LRG_475:g.13671G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361866.8:c.999G>T MANE Select | ENSP00000355180.3:p.Val333= | |
| ENST00000361866.7:c.999G>T | ENSP00000355180.3:p.Val333= | |
| ENST00000612273.1:c.999G>T | ENSP00000483630.1:p.Val333= | |
| NM_001848.2:c.999G>T , LRG_475t1:c.999G>T | NP_001839.2:p.Val333= | |
| NM_001848.3:c.999G>T MANE Select | NP_001839.2:p.Val333= |