Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.3082669C>A , CM000682.2:g.3082669C>A | GRCh38 |
| NC_000020.10:g.3063315C>A , CM000682.1:g.3063315C>A | GRCh37 |
| NC_000020.9:g.3011315C>A | NCBI36 |
| NG_008663.1:g.7056G>T , LRG_715:g.7056G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380293.3:c.456G>T MANE Select | ENSP00000369647.3:p.Ala152= | |
| NM_000490.4:c.456G>T , LRG_715t1:c.456G>T | NP_000481.2:p.Ala152= | |
| XM_011529267.1:c.456G>T | XP_011527569.1:p.Ala152= | |
| XM_011529267.2:c.456G>T | XP_011527569.1:p.Ala152= | |
| NM_000490.5:c.456G>T MANE Select | NP_000481.2:p.Ala152= |