Linked Data
dbSNP Id:
rs1284697900
gnomAD v3:
11-118491026-A-G
gnomAD v4:
11-118491026-A-G
MyVariant Identifiers:
chr11:g.118491026A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118491026A>G , CM000673.2:g.118491026A>G | GRCh38 |
| NC_000011.9:g.118361741A>G , CM000673.1:g.118361741A>G | GRCh37 |
| NC_000011.8:g.117866951A>G | NCBI36 |
| NG_027813.1:g.59537A>G , LRG_613:g.59537A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000531904.7:c.4796-170A>G | ENSP00000432391.3:n.4796-170A>G | |
| ENST00000710560.1:c.4796-170A>G | ENSP00000518343.1:n.4796-170A>G | |
| ENST00000685498.1:c.473-170A>G | ENSP00000509293.1:n.473-170A>G | |
| ENST00000691053.1:c.4697-170A>G | ENSP00000509168.1:n.4697-170A>G | |
| ENST00000389506.10:c.4697-170A>G | ENSP00000374157.5:n.4697-170A>G | |
| ENST00000534358.8:c.4697-170A>G MANE Select | ENSP00000436786.2:n.4697-170A>G | |
| ENST00000649699.1:c.4583-170A>G | ENSP00000496927.1:n.4583-170A>G | |
| ENST00000389506.9:c.4697-170A>G | ENSP00000374157.5:n.4697-170A>G | |
| ENST00000392873.3:c.833-170A>G | ENSP00000376612.3:n.833-170A>G | |
| ENST00000534358.5:c.4697-170A>G | ENSP00000436786.1:n.4697-170A>G | |
| NM_001197104.1:c.4697-170A>G , LRG_613t1:c.4697-170A>G | NP_001184033.1:n.4697-170A>G | |
| NM_005933.3:c.4697-170A>G | NP_005924.2:n.4697-170A>G | |
| XM_006718839.2:c.2180-170A>G | XP_006718902.2:n.2180-170A>G | |
| XM_011542829.1:c.4796-170A>G | XP_011541131.1:n.4796-170A>G | |
| XM_011542830.1:c.4793-170A>G | XP_011541132.1:n.4793-170A>G | |
| XM_011542831.1:c.4796-170A>G | XP_011541133.1:n.4796-170A>G | |
| XM_011542832.1:c.2603-170A>G | XP_011541134.1:n.2603-170A>G | |
| XM_011542833.1:c.2279-170A>G | XP_011541135.1:n.2279-170A>G | |
| XM_006718839.3:c.2180-170A>G | XP_006718902.2:n.2180-170A>G | |
| XM_011542829.2:c.4796-170A>G | XP_011541131.1:n.4796-170A>G | |
| XM_011542830.2:c.4793-170A>G | XP_011541132.1:n.4793-170A>G | |
| XM_011542831.2:c.4796-170A>G | XP_011541133.1:n.4796-170A>G | |
| XM_011542833.2:c.2279-170A>G | XP_011541135.1:n.2279-170A>G | |
| NM_001197104.2:c.4697-170A>G MANE Select | NP_001184033.1:n.4697-170A>G | |
| NM_005933.4:c.4697-170A>G | NP_005924.2:n.4697-170A>G |