Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110589926G>T , CM000672.2:g.110589926G>T | GRCh38 |
| NC_000010.10:g.112349684G>T , CM000672.1:g.112349684G>T | GRCh37 |
| NC_000010.9:g.112339674G>T | NCBI36 |
| NG_012217.1:g.27236G>T , LRG_774:g.27236G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684797.1:n.1344G>T | ||
| ENST00000684988.1:n.2089G>T | ||
| ENST00000687823.1:n.1358G>T | ||
| ENST00000689932.1:n.3507G>T | ||
| ENST00000691297.1:n.1577G>T | ||
| ENST00000691527.1:n.2247G>T | ||
| ENST00000692792.1:n.1563G>T | ||
| ENST00000361804.5:c.1444G>T MANE Select | ENSP00000354720.5:p.Ala482Ser | |
| ENST00000361804.4:c.1444G>T | ENSP00000354720.4:p.Ala482Ser | |
| NM_005445.3:c.1444G>T , LRG_774t1:c.1444G>T | NP_005436.1:p.Ala482Ser | |
| NM_005445.4:c.1444G>T MANE Select | NP_005436.1:p.Ala482Ser |