Linked Data
dbSNP Id:
rs564590358
gnomAD v2:
5-176520183-A-T
gnomAD v3:
5-177093182-A-T
gnomAD v4:
5-177093182-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.177093182A>T , CM000667.2:g.177093182A>T | GRCh38 |
| NC_000005.9:g.176520183A>T , CM000667.1:g.176520183A>T | GRCh37 |
| NC_000005.8:g.176452789A>T | NCBI36 |
| NG_012067.1:g.11263A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000292408.9:c.1102A>T MANE Select | ENSP00000292408.4:p.Thr368Ser | |
| ENST00000292408.8:c.1102A>T | ENSP00000292408.4:p.Thr368Ser | |
| ENST00000393637.5:c.1058-150A>T | ENSP00000377254.1:n.1058-150A>T | |
| ENST00000393648.6:c.1097+5A>T | ENSP00000377259.2:n.1097+5A>T | |
| ENST00000502906.5:c.1102A>T | ENSP00000424960.1:p.Thr368Ser | |
| ENST00000508139.1:n.406A>T | ||
| ENST00000511076.1:c.8A>T | ||
| NM_001291980.1:c.1097+5A>T | NP_001278909.1:n.1097+5A>T | |
| NM_002011.4:c.1102A>T | NP_002002.3:p.Thr368Ser | |
| NM_022963.3:c.1058-150A>T | NP_075252.2:n.1058-150A>T | |
| NM_213647.2:c.1102A>T | NP_998812.1:p.Thr368Ser | |
| XM_005265838.2:c.1102A>T | XP_005265895.1:p.Thr368Ser | |
| XM_011534464.1:c.1195A>T | XP_011532766.1:p.Thr399Ser | |
| XM_011534465.1:c.784A>T | XP_011532767.1:p.Thr262Ser | |
| XR_941090.1:n.1147A>T | ||
| NM_001354984.1:c.1102A>T | NP_001341913.1:p.Thr368Ser | |
| NM_213647.3:c.1102A>T MANE Select | NP_998812.1:p.Thr368Ser | |
| NM_001291980.2:c.1097+5A>T | NP_001278909.1:n.1097+5A>T | |
| NM_001354984.2:c.1102A>T | NP_001341913.1:p.Thr368Ser | |
| NM_002011.5:c.1102A>T | NP_002002.3:p.Thr368Ser |