Linked Data
ClinVar Variation Id:
21484
dbSNP Id:
rs80356721
ExAC:
1:11082347 G / T
gnomAD v2:
1-11082347-G-T
gnomAD v3:
1-11022290-G-T
gnomAD v4:
1-11022290-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11022290G>T , CM000663.2:g.11022290G>T | GRCh38 |
| NC_000001.10:g.11082347G>T , CM000663.1:g.11082347G>T | GRCh37 |
| NC_000001.9:g.11004934G>T | NCBI36 |
| NG_008734.1:g.14669G>T , LRG_659:g.14669G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700088.1:c.1397-97C>A (MASP2) | ENSP00000514787.1:n.1397-97C>A | |
| ENST00000240185.8:c.881G>T (TARDBP) MANE Select | ENSP00000240185.4:p.Gly294Val | |
| ENST00000639083.1:c.881G>T (TARDBP) | ENSP00000491203.1:p.Gly294Val | |
| ENST00000639599.1:c.832+49G>T (TARDBP) | ENSP00000492196.1:n.832+49G>T | |
| ENST00000649624.1:c.768+113G>T (TARDBP) | ENSP00000497327.1:n.768+113G>T | |
| ENST00000240185.7:c.881G>T (TARDBP) | ENSP00000240185.3:p.Gly294Val | |
| ENST00000315091.7:c.832+49G>T (TARDBP) | ENSP00000313129.3:n.832+49G>T | |
| ENST00000439080.6:c.*462G>T (TARDBP) | ENSP00000404666.3:n.*462G>T | |
| ENST00000473869.5:c.841+40G>T (TARDBP) | ENSP00000432132.1:n.841+40G>T | |
| ENST00000477447.6:c.140+40G>T (TARDBP) | ||
| ENST00000610369.4:c.319+40G>T (TARDBP) | ENSP00000482559.1:n.319+40G>T | |
| ENST00000611136.4:c.212+49G>T | ||
| ENST00000611963.4:c.472+49G>T (TARDBP) | ENSP00000481330.1:n.472+49G>T | |
| ENST00000612542.1:c.107+40G>T | ||
| ENST00000614494.1:c.221+113G>T (TARDBP) | ||
| ENST00000614757.4:c.841+40G>T | ENSP00000481867.1:n.841+40G>T | |
| ENST00000616545.4:c.841+40G>T (TARDBP) | ENSP00000484722.1:n.841+40G>T | |
| ENST00000617172.4:c.582+40G>T (TARDBP) | ||
| ENST00000619555.4:c.392+40G>T (TARDBP) | ||
| ENST00000620632.4:c.392+40G>T (TARDBP) | ||
| ENST00000621715.4:c.710G>T (TARDBP) | ENSP00000480690.1:p.Gly237Val | |
| ENST00000621790.4:c.859+22G>T (TARDBP) | ENSP00000482191.1:n.859+22G>T | |
| ENST00000622057.4:c.579+49G>T (TARDBP) | ||
| ENST00000629725.2:c.841+40G>T (TARDBP) | ENSP00000486989.1:n.841+40G>T | |
| NM_007375.3:c.881G>T , LRG_659t1:c.881G>T (TARDBP) | NP_031401.1:p.Gly294Val | |
| XR_946596.1:n.1003G>T (TARDBP) | ||
| XR_946597.1:n.1003G>T (TARDBP) | ||
| XM_017000863.2:c.881G>T (TARDBP) | XP_016856352.1:p.Gly294Val | |
| XM_017000864.2:c.881G>T (TARDBP) | XP_016856353.1:p.Gly294Val | |
| XM_017000865.2:c.881G>T (TARDBP) | XP_016856354.1:p.Gly294Val | |
| XM_017000866.2:c.881G>T (TARDBP) | XP_016856355.1:p.Gly294Val | |
| XM_017000867.2:c.881G>T (TARDBP) | XP_016856356.1:p.Gly294Val | |
| XM_017000868.2:c.881G>T (TARDBP) | XP_016856357.1:p.Gly294Val | |
| NM_007375.4:c.881G>T (TARDBP) MANE Select | NP_031401.1:p.Gly294Val |