Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42536567T>A , CM000679.2:g.42536567T>A | GRCh38 |
| NC_000017.10:g.40688585T>A , CM000679.1:g.40688585T>A | GRCh37 |
| NC_000017.9:g.37942111T>A | NCBI36 |
| NG_011552.1:g.5635T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.295T>A MANE Select | ENSP00000225927.1:p.Cys99Ser | |
| ENST00000225927.6:c.295T>A | ENSP00000225927.1:p.Cys99Ser | |
| ENST00000586516.5:c.45T>A | ||
| ENST00000591587.1:c.38T>A | ENSP00000467836.1:p.Leu13Gln | |
| NM_000263.3:c.295T>A | NP_000254.2:p.Cys99Ser | |
| XM_006721920.2:c.-448T>A | XP_006721983.1:n.-448T>A | |
| XM_011524840.1:c.-448T>A | XP_011523142.1:n.-448T>A | |
| XM_024450771.1:c.295T>A | XP_024306539.1:p.Cys99Ser | |
| NM_000263.4:c.295T>A MANE Select | NP_000254.2:p.Cys99Ser |