Linked Data
dbSNP Id:
rs1057521146
gnomAD v2:
17-78190950-C-T
gnomAD v3:
17-80217151-C-T
gnomAD v4:
17-80217151-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.80217151C>T , CM000679.2:g.80217151C>T | GRCh38 |
| NC_000017.10:g.78190950C>T , CM000679.1:g.78190950C>T | GRCh37 |
| NC_000017.9:g.75805545C>T | NCBI36 |
| NG_008229.1:g.8250G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000326317.11:c.130G>A MANE Select | ENSP00000314606.6:p.Ala44Thr | |
| ENST00000326317.10:c.130G>A | ENSP00000314606.6:p.Ala44Thr | |
| ENST00000570427.1:c.130G>A | ENSP00000459765.1:p.Ala44Thr | |
| ENST00000570923.1:c.165G>A | ENSP00000458200.1:p.Ala55= | |
| ENST00000571051.5:n.150G>A | ||
| ENST00000571075.1:n.150G>A | ||
| ENST00000571675.5:n.150G>A | ||
| ENST00000572208.5:n.148G>A | ||
| ENST00000573150.5:c.130G>A | ENSP00000459280.1:p.Ala44Thr | |
| ENST00000574505.5:c.75G>A | ||
| ENST00000575188.5:n.150G>A | ||
| ENST00000575282.5:n.139G>A | ||
| ENST00000576707.5:c.-132G>A | ENSP00000461128.1:n.-132G>A | |
| ENST00000576941.5:c.130G>A | ENSP00000461160.1:p.Ala44Thr | |
| NM_000199.3:c.130G>A | NP_000190.1:p.Ala44Thr | |
| XM_005257582.2:c.130G>A | XP_005257639.1:p.Ala44Thr | |
| XM_005257583.3:c.130G>A | XP_005257640.1:p.Ala44Thr | |
| XM_011525126.1:c.130G>A | XP_011523428.1:p.Ala44Thr | |
| XM_011525127.1:c.130G>A | XP_011523429.1:p.Ala44Thr | |
| XR_934532.1:n.150G>A | ||
| NM_000199.4:c.130G>A | NP_000190.1:p.Ala44Thr | |
| NM_001352921.1:c.130G>A | NP_001339850.1:p.Ala44Thr | |
| NM_001352922.1:c.130G>A | NP_001339851.1:p.Ala44Thr | |
| NR_148201.1:n.217G>A | ||
| XM_005257583.4:c.130G>A | XP_005257640.1:p.Ala44Thr | |
| XM_017024952.1:c.130G>A | XP_016880441.1:p.Ala44Thr | |
| XR_001752585.1:n.150G>A | ||
| XR_001752586.1:n.150G>A | ||
| XR_001752587.1:n.150G>A | ||
| XR_001752588.1:n.150G>A | ||
| XR_001752589.1:n.150G>A | ||
| XR_001752590.1:n.150G>A | ||
| XR_001752591.1:n.150G>A | ||
| XR_001752592.1:n.150G>A | ||
| XR_002958057.1:n.150G>A | ||
| XR_934532.2:n.150G>A | ||
| NM_000199.5:c.130G>A MANE Select | NP_000190.1:p.Ala44Thr | |
| NM_001352921.2:c.130G>A | NP_001339850.1:p.Ala44Thr | |
| NM_001352922.2:c.130G>A | NP_001339851.1:p.Ala44Thr | |
| NR_148201.2:n.150G>A | ||
| NM_001352921.3:c.130G>A | NP_001339850.1:p.Ala44Thr |