Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42544219G>C , CM000679.2:g.42544219G>C | GRCh38 |
| NC_000017.10:g.40696237G>C , CM000679.1:g.40696237G>C | GRCh37 |
| NC_000017.9:g.37949763G>C | NCBI36 |
| NG_011552.1:g.13287G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.2213G>C MANE Select | ENSP00000225927.1:p.Trp738Ser | |
| ENST00000225927.6:c.2213G>C | ENSP00000225927.1:p.Trp738Ser | |
| NM_000263.3:c.2213G>C | NP_000254.2:p.Trp738Ser | |
| XM_006721920.2:c.1382G>C | XP_006721983.1:p.Trp461Ser | |
| XM_011524840.1:c.1214G>C | XP_011523142.1:p.Trp405Ser | |
| XM_017024687.1:c.1382G>C | XP_016880176.1:p.Trp461Ser | |
| XM_024450771.1:c.2270G>C | XP_024306539.1:p.Trp757Ser | |
| XM_024450772.1:c.1214G>C | XP_024306540.1:p.Trp405Ser | |
| NM_000263.4:c.2213G>C MANE Select | NP_000254.2:p.Trp738Ser |