Linked Data
ClinVar Variation Id:
461148
dbSNP Id:
rs786202549
gnomAD v3:
17-61683658-T-C
gnomAD v4:
17-61683658-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.61683658T>C , CM000679.2:g.61683658T>C | GRCh38 |
| NC_000017.10:g.59761019T>C , CM000679.1:g.59761019T>C | GRCh37 |
| NC_000017.9:g.57115801T>C | NCBI36 |
| NG_007409.2:g.184902A>G , LRG_300:g.184902A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682073.1:n.2128A>G | ||
| ENST00000682453.1:c.3388A>G | ENSP00000506943.1:p.Ile1130Val | |
| ENST00000682477.1:c.*2814A>G | ENSP00000507075.1:n.*2814A>G | |
| ENST00000682589.1:n.9265A>G | ||
| ENST00000682755.1:c.3166A>G | ENSP00000507660.1:p.Ile1056Val | |
| ENST00000682989.1:c.*479A>G | ENSP00000507786.1:n.*479A>G | |
| ENST00000683039.1:c.3388A>G | ENSP00000508303.1:p.Ile1130Val | |
| ENST00000683235.1:c.*803A>G | ENSP00000507646.1:n.*803A>G | |
| ENST00000683535.1:n.1518A>G | ||
| ENST00000684584.1:c.2551A>G | ENSP00000508044.1:p.Ile851Val | |
| ENST00000684626.1:n.1634A>G | ||
| ENST00000684769.1:c.1578A>G | ENSP00000507691.1:n.1578A>G | |
| ENST00000259008.7:c.3388A>G MANE Select | ENSP00000259008.2:p.Ile1130Val | |
| ENST00000259008.6:c.3388A>G | ENSP00000259008.2:p.Ile1130Val | |
| NM_032043.2:c.3388A>G , LRG_300t1:c.3388A>G | NP_114432.2:p.Ile1130Val | |
| XM_011525332.1:c.3448A>G | XP_011523634.1:p.Ile1150Val | |
| XM_011525333.1:c.3448A>G | XP_011523635.1:p.Ile1150Val | |
| XM_011525334.1:c.3448A>G | XP_011523636.1:p.Ile1150Val | |
| XM_011525335.1:c.3388A>G | XP_011523637.1:p.Ile1130Val | |
| XM_011525336.1:c.3328A>G | XP_011523638.1:p.Ile1110Val | |
| XM_011525337.1:c.3247A>G | XP_011523639.1:p.Ile1083Val | |
| XM_011525338.1:c.2965A>G | XP_011523640.1:p.Ile989Val | |
| XM_011525332.3:c.3448A>G | XP_011523634.1:p.Ile1150Val | |
| XM_011525333.3:c.3448A>G | XP_011523635.1:p.Ile1150Val | |
| XM_011525334.2:c.3448A>G | XP_011523636.1:p.Ile1150Val | |
| XM_011525335.3:c.3388A>G | XP_011523637.1:p.Ile1130Val | |
| XM_011525336.2:c.3328A>G | XP_011523638.1:p.Ile1110Val | |
| XM_011525337.2:c.3247A>G | XP_011523639.1:p.Ile1083Val | |
| XM_011525338.2:c.2965A>G | XP_011523640.1:p.Ile989Val | |
| XM_017025200.1:c.2905A>G | XP_016880689.1:p.Ile969Val | |
| XM_017025201.1:c.2905A>G | XP_016880690.1:p.Ile969Val | |
| XM_017025202.1:c.1534A>G | XP_016880691.1:p.Ile512Val | |
| XM_017025203.1:c.1534A>G | XP_016880692.1:p.Ile512Val | |
| NM_032043.3:c.3388A>G MANE Select | NP_114432.2:p.Ile1130Val |