Linked Data
ClinVar Variation Id:
306599
dbSNP Id:
rs759550730
ExAC:
11:9875226 T / C
gnomAD v2:
11-9875226-T-C
gnomAD v3:
11-9853679-T-C
gnomAD v4:
11-9853679-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.9853679T>C , CM000673.2:g.9853679T>C | GRCh38 |
| NC_000011.9:g.9875226T>C , CM000673.1:g.9875226T>C | GRCh37 |
| NC_000011.8:g.9831802T>C | NCBI36 |
| NG_008074.1:g.445529A>G , LRG_267:g.445529A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000420722.3:c.1101A>G | ENSP00000410478.3:p.Thr367= | |
| ENST00000530741.2:c.1101A>G | ENSP00000432643.2:p.Thr367= | |
| ENST00000533770.6:c.2397A>G | ENSP00000509247.1:p.Thr799= | |
| ENST00000675281.2:c.2397A>G | ENSP00000502491.1:p.Thr799= | |
| ENST00000676324.2:c.2397A>G | ENSP00000502578.1:p.Thr799= | |
| ENST00000676387.2:c.2283A>G | ENSP00000502779.1:p.Thr761= | |
| ENST00000687210.1:c.*1019A>G | ENSP00000509480.1:n.*1019A>G | |
| ENST00000688344.1:c.2004A>G | ENSP00000509987.1:p.Thr668= | |
| ENST00000688417.1:n.2547A>G | ||
| ENST00000689128.1:c.2397A>G | ENSP00000509587.1:p.Thr799= | |
| ENST00000689258.1:c.2259A>G | ENSP00000510475.1:p.Thr753= | |
| ENST00000689597.1:c.1101A>G | ENSP00000510781.1:p.Thr367= | |
| ENST00000689674.1:c.1101A>G | ENSP00000510723.1:p.Thr367= | |
| ENST00000689940.1:c.2391A>G | ENSP00000508452.1:p.Thr797= | |
| ENST00000690003.1:c.1101A>G | ENSP00000508748.1:p.Thr367= | |
| ENST00000692716.1:c.2268A>G | ENSP00000509545.1:p.Thr756= | |
| ENST00000693181.1:c.1101A>G | ENSP00000510179.1:p.Thr367= | |
| ENST00000256190.13:c.2397A>G MANE Select | ENSP00000256190.8:p.Thr799= | |
| ENST00000675281.1:c.2397A>G | ENSP00000502491.1:p.Thr799= | |
| ENST00000676324.1:c.2397A>G | ENSP00000502578.1:p.Thr799= | |
| ENST00000676387.1:c.2283A>G | ENSP00000502779.1:p.Thr761= | |
| ENST00000256190.12:c.2397A>G | ENSP00000256190.8:p.Thr799= | |
| ENST00000533770.5:n.2312A>G | ||
| ENST00000617179.4:c.2256A>G | ENSP00000482806.1:p.Thr752= | |
| NM_030962.3:c.2397A>G , LRG_267t1:c.2397A>G | NP_112224.1:p.Thr799= | |
| NR_120539.1:n.135+14403T>C | ||
| XM_005253154.3:c.2397A>G | XP_005253211.1:p.Thr799= | |
| XM_005253155.3:c.2268A>G | XP_005253212.1:p.Thr756= | |
| XM_011520394.1:c.2283A>G | XP_011518696.1:p.Thr761= | |
| XM_011520395.1:c.2397A>G | XP_011518697.1:p.Thr799= | |
| XM_011520396.1:c.2397A>G | XP_011518698.1:p.Thr799= | |
| XM_005253154.5:c.2397A>G | XP_005253211.1:p.Thr799= | |
| XM_005253155.5:c.2268A>G | XP_005253212.1:p.Thr756= | |
| XM_011520394.3:c.2283A>G | XP_011518696.1:p.Thr761= | |
| XM_011520395.3:c.2397A>G | XP_011518697.1:p.Thr799= | |
| XM_011520396.3:c.2397A>G | XP_011518698.1:p.Thr799= | |
| XM_017018372.2:c.2259A>G | XP_016873861.1:p.Thr753= | |
| XM_017018373.2:c.2259A>G | XP_016873862.1:p.Thr753= | |
| XM_017018374.2:c.2268A>G | XP_016873863.1:p.Thr756= | |
| XM_017018375.2:c.2397A>G | XP_016873864.1:p.Thr799= | |
| XM_017018376.2:c.2397A>G | XP_016873865.1:p.Thr799= | |
| XM_017018377.2:c.2397A>G | XP_016873866.1:p.Thr799= | |
| XR_001747994.2:n.2535A>G | ||
| NM_001386339.1:c.2397A>G | NP_001373268.1:p.Thr799= | |
| NM_001386342.1:c.2268A>G | NP_001373271.1:p.Thr756= | |
| NM_030962.4:c.2397A>G MANE Select | NP_112224.1:p.Thr799= |