Linked Data
ClinVar Variation Id:
241768
dbSNP Id:
rs149228565
ExAC:
17:56772404 A / T
gnomAD v2:
17-56772404-A-T
gnomAD v3:
17-58695043-A-T
gnomAD v4:
17-58695043-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58695043A>T , CM000679.2:g.58695043A>T | GRCh38 |
| NC_000017.10:g.56772404A>T , CM000679.1:g.56772404A>T | GRCh37 |
| NC_000017.9:g.54127403A>T | NCBI36 |
| NG_023199.1:g.7442A>T , LRG_314:g.7442A>T | |
| NG_047169.1:g.2037T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461271.6:c.-94A>T | ENSP00000464056.2:n.-94A>T | |
| ENST00000697675.1:n.1352A>T | ||
| ENST00000697676.1:n.318A>T | ||
| ENST00000697677.1:n.1339A>T | ||
| ENST00000697678.1:n.160A>T | ||
| ENST00000697679.1:n.1332A>T | ||
| ENST00000697680.1:c.*1122A>T | ENSP00000513392.1:n.*1122A>T | |
| ENST00000697681.1:c.*1122A>T | ENSP00000513393.1:n.*1122A>T | |
| ENST00000697683.1:c.*1122A>T | ENSP00000513395.1:n.*1122A>T | |
| ENST00000697684.1:n.318A>T | ||
| ENST00000697685.1:c.*1122A>T | ENSP00000513396.1:n.*1122A>T | |
| ENST00000697686.1:c.-94A>T | ENSP00000513397.1:n.-94A>T | |
| ENST00000697687.1:n.304A>T | ||
| ENST00000697688.1:n.304A>T | ||
| ENST00000697689.1:c.*961A>T | ENSP00000513398.1:n.*961A>T | |
| ENST00000697690.1:c.258A>T | ENSP00000513399.1:p.Thr86= | |
| ENST00000697691.1:c.*230A>T | ENSP00000513400.1:n.*230A>T | |
| ENST00000697692.1:c.*270A>T | ENSP00000513401.1:n.*270A>T | |
| ENST00000697693.1:n.1033A>T | ||
| ENST00000697694.1:c.-94A>T | ENSP00000513402.1:n.-94A>T | |
| ENST00000697695.1:n.865A>T | ||
| ENST00000337432.9:c.258A>T MANE Select | ENSP00000336701.4:p.Thr86= | |
| ENST00000337432.8:c.258A>T | ENSP00000336701.4:p.Thr86= | |
| ENST00000421782.3:c.258A>T | ENSP00000391450.2:p.Thr86= | |
| ENST00000425173.5:c.54A>T | ENSP00000407282.1:p.Thr18= | |
| ENST00000461271.5:c.-94A>T | ENSP00000464056.1:n.-94A>T | |
| ENST00000475762.5:c.*961A>T | ENSP00000432421.1:n.*961A>T | |
| ENST00000482007.5:c.258A>T | ENSP00000433332.1:p.Thr86= | |
| ENST00000486827.1:c.*1122A>T | ENSP00000436761.1:n.*1122A>T | |
| ENST00000487525.5:c.258A>T | ENSP00000431637.1:p.Thr86= | |
| ENST00000487921.5:n.170A>T | ||
| ENST00000583539.5:c.258A>T | ENSP00000463121.1:p.Thr86= | |
| ENST00000584617.5:c.127-1650A>T | ||
| NM_002876.3:c.258A>T | NP_002867.1:p.Thr86= | |
| NM_058216.2:c.258A>T | NP_478123.1:p.Thr86= | |
| NR_103872.1:n.329A>T | ||
| NR_103873.1:n.226A>T | ||
| XM_006722001.2:c.258A>T | XP_006722064.1:p.Thr86= | |
| XM_006722002.2:c.258A>T | XP_006722065.1:p.Thr86= | |
| XM_006722004.2:c.-94A>T | XP_006722067.1:n.-94A>T | |
| XM_006722005.2:c.-94A>T | XP_006722068.1:n.-94A>T | |
| XM_011525092.1:c.-94A>T | XP_011523394.1:n.-94A>T | |
| XM_011525093.1:c.-94A>T | XP_011523395.1:n.-94A>T | |
| XM_011525094.1:c.-94A>T | XP_011523396.1:n.-94A>T | |
| XR_934513.1:n.331A>T | ||
| XR_934514.1:n.331A>T | ||
| XM_006722001.4:c.258A>T | XP_006722064.1:p.Thr86= | |
| XM_006722002.4:c.258A>T | XP_006722065.1:p.Thr86= | |
| XM_006722004.3:c.-94A>T | XP_006722067.1:n.-94A>T | |
| XM_006722005.3:c.-94A>T | XP_006722068.1:n.-94A>T | |
| XM_011525092.2:c.-94A>T | XP_011523394.1:n.-94A>T | |
| XM_011525093.2:c.-94A>T | XP_011523395.1:n.-94A>T | |
| XM_011525094.2:c.-94A>T | XP_011523396.1:n.-94A>T | |
| XM_017024914.1:c.-94A>T | XP_016880403.1:n.-94A>T | |
| XM_017024915.1:c.-94A>T | XP_016880404.1:n.-94A>T | |
| XM_017024916.1:c.-94A>T | XP_016880405.1:n.-94A>T | |
| XM_017024917.1:c.-94A>T | XP_016880406.1:n.-94A>T | |
| XM_017024918.2:c.-94A>T | XP_016880407.1:n.-94A>T | |
| XM_017024919.1:c.-94A>T | XP_016880408.1:n.-94A>T | |
| XR_934513.3:n.762A>T | ||
| XR_934514.3:n.762A>T | ||
| NM_058216.3:c.258A>T MANE Select | NP_478123.1:p.Thr86= | |
| NR_103872.2:n.300A>T | ||
| NM_002876.4:c.258A>T | NP_002867.1:p.Thr86= |