Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.5603268T>A , CM000669.2:g.5603268T>A | GRCh38 |
| NC_000007.13:g.5642899T>A , CM000669.1:g.5642899T>A | GRCh37 |
| NC_000007.12:g.5609425T>A | NCBI36 |
| NG_030004.1:g.15464T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382361.8:c.844T>A MANE Select | ENSP00000371798.3:p.Ser282Thr | |
| ENST00000382361.7:c.844T>A | ENSP00000371798.3:p.Ser282Thr | |
| ENST00000405801.2:c.10T>A | ENSP00000383982.2:p.Ser4Thr | |
| ENST00000444748.5:c.10T>A | ENSP00000404506.1:p.Ser4Thr | |
| ENST00000447103.5:c.10T>A | ENSP00000409967.1:p.Ser4Thr | |
| ENST00000473330.1:n.397T>A | ||
| NM_003088.3:c.844T>A | NP_003079.1:p.Ser282Thr | |
| NM_003088.4:c.844T>A MANE Select | NP_003079.1:p.Ser282Thr |