Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.48527214G>T , CM000685.2:g.48527214G>T | GRCh38 |
| NC_000023.10:g.48385602G>T , CM000685.1:g.48385602G>T | GRCh37 |
| NC_000023.9:g.48270546G>T | NCBI36 |
| NG_007452.1:g.10439G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000495186.6:c.398G>T MANE Select | ENSP00000417052.1:p.Ser133Ile | |
| ENST00000651615.1:c.398G>T | ENSP00000498524.1:p.Ser133Ile | |
| ENST00000276096.10:n.356G>T | ||
| ENST00000414061.1:c.398G>T | ENSP00000405832.1:p.Ser133Ile | |
| ENST00000446158.5:c.398G>T | ENSP00000390031.1:p.Ser133Ile | |
| ENST00000466461.1:n.237G>T | ||
| ENST00000495186.5:c.398G>T | ENSP00000417052.1:p.Ser133Ile | |
| ENST00000498425.1:n.519G>T | ||
| NM_006579.2:c.398G>T | NP_006570.1:p.Ser133Ile | |
| NM_006579.3:c.398G>T MANE Select | NP_006570.1:p.Ser133Ile |