Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229431635G>A , CM000663.2:g.229431635G>A | GRCh38 |
| NC_000001.10:g.229567382G>A , CM000663.1:g.229567382G>A | GRCh37 |
| NC_000001.9:g.227634005G>A | NCBI36 |
| NG_006672.1:g.7462C>T , LRG_429:g.7462C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000366683.4:c.991-71C>T | ENSP00000355644.4:n.991-71C>T | |
| ENST00000684723.1:c.863C>T | ENSP00000508084.1:p.Ala288Val | |
| ENST00000366683.3:c.629C>T | ENSP00000355644.3:p.Ala210Val | |
| ENST00000366684.7:c.998C>T MANE Select | ENSP00000355645.3:p.Ala333Val | |
| NM_001100.3:c.998C>T , LRG_429t1:c.998C>T | NP_001091.1:p.Ala333Val | |
| NM_001100.4:c.998C>T MANE Select | NP_001091.1:p.Ala333Val |