Linked Data
dbSNP Id:
rs895315134
gnomAD v4:
11-118491044-C-T
MyVariant Identifiers:
chr11:g.118491044C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118491044C>T , CM000673.2:g.118491044C>T | GRCh38 |
| NC_000011.9:g.118361759C>T , CM000673.1:g.118361759C>T | GRCh37 |
| NC_000011.8:g.117866969C>T | NCBI36 |
| NG_027813.1:g.59555C>T , LRG_613:g.59555C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000531904.7:c.4796-152C>T | ENSP00000432391.3:n.4796-152C>T | |
| ENST00000710560.1:c.4796-152C>T | ENSP00000518343.1:n.4796-152C>T | |
| ENST00000685498.1:c.473-152C>T | ENSP00000509293.1:n.473-152C>T | |
| ENST00000691053.1:c.4697-152C>T | ENSP00000509168.1:n.4697-152C>T | |
| ENST00000389506.10:c.4697-152C>T | ENSP00000374157.5:n.4697-152C>T | |
| ENST00000534358.8:c.4697-152C>T MANE Select | ENSP00000436786.2:n.4697-152C>T | |
| ENST00000649699.1:c.4583-152C>T | ENSP00000496927.1:n.4583-152C>T | |
| ENST00000389506.9:c.4697-152C>T | ENSP00000374157.5:n.4697-152C>T | |
| ENST00000392873.3:c.833-152C>T | ENSP00000376612.3:n.833-152C>T | |
| ENST00000534358.5:c.4697-152C>T | ENSP00000436786.1:n.4697-152C>T | |
| NM_001197104.1:c.4697-152C>T , LRG_613t1:c.4697-152C>T | NP_001184033.1:n.4697-152C>T | |
| NM_005933.3:c.4697-152C>T | NP_005924.2:n.4697-152C>T | |
| XM_006718839.2:c.2180-152C>T | XP_006718902.2:n.2180-152C>T | |
| XM_011542829.1:c.4796-152C>T | XP_011541131.1:n.4796-152C>T | |
| XM_011542830.1:c.4793-152C>T | XP_011541132.1:n.4793-152C>T | |
| XM_011542831.1:c.4796-152C>T | XP_011541133.1:n.4796-152C>T | |
| XM_011542832.1:c.2603-152C>T | XP_011541134.1:n.2603-152C>T | |
| XM_011542833.1:c.2279-152C>T | XP_011541135.1:n.2279-152C>T | |
| XM_006718839.3:c.2180-152C>T | XP_006718902.2:n.2180-152C>T | |
| XM_011542829.2:c.4796-152C>T | XP_011541131.1:n.4796-152C>T | |
| XM_011542830.2:c.4793-152C>T | XP_011541132.1:n.4793-152C>T | |
| XM_011542831.2:c.4796-152C>T | XP_011541133.1:n.4796-152C>T | |
| XM_011542833.2:c.2279-152C>T | XP_011541135.1:n.2279-152C>T | |
| NM_001197104.2:c.4697-152C>T MANE Select | NP_001184033.1:n.4697-152C>T | |
| NM_005933.4:c.4697-152C>T | NP_005924.2:n.4697-152C>T |