Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47744824T>G , CM000679.2:g.47744824T>G | GRCh38 |
| NC_000017.10:g.45822190T>G , CM000679.1:g.45822190T>G | GRCh37 |
| NC_000017.9:g.43177189T>G | NCBI36 |
| NG_012166.1:g.16581T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000177694.2:c.1066T>G MANE Select | ENSP00000177694.1:p.Ser356Ala | |
| ENST00000177694.1:c.1066T>G | ENSP00000177694.1:p.Ser356Ala | |
| NM_013351.1:c.1066T>G | NP_037483.1:p.Ser356Ala | |
| XM_011524698.1:c.1129T>G | XP_011523000.1:p.Ser377Ala | |
| XM_011524699.1:c.733T>G | XP_011523001.1:p.Ser245Ala | |
| NM_013351.2:c.1066T>G MANE Select | NP_037483.1:p.Ser356Ala |