Linked Data
ClinVar Variation Id:
413155
dbSNP Id:
rs372356060
ExAC:
2:179515989 T / C
gnomAD v2:
2-179515989-T-C
gnomAD v3:
2-178651262-T-C
gnomAD v4:
2-178651262-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178651262T>C , CM000664.2:g.178651262T>C | GRCh38 |
| NC_000002.11:g.179515989T>C , CM000664.1:g.179515989T>C | GRCh37 |
| NC_000002.10:g.179224234T>C | NCBI36 |
| NG_011618.3:g.184541A>G , LRG_391:g.184541A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.32304A>G | ENSP00000343764.6:p.Pro10768= | |
| ENST00000342175.11:c.13859-8945A>G | ENSP00000340554.6:n.13859-8945A>G | |
| ENST00000359218.10:c.13658-8945A>G | ENSP00000352154.5:n.13658-8945A>G | |
| ENST00000342175.10:c.13859-8945A>G | ENSP00000340554.6:n.13859-8945A>G | |
| ENST00000342992.10:c.32304A>G | ENSP00000343764.6:p.Pro10768= | |
| ENST00000359218.9:c.13658-8945A>G | ENSP00000352154.5:n.13658-8945A>G | |
| ENST00000414766.5:c.2441-8945A>G | ENSP00000401501.1:n.2441-8945A>G | |
| ENST00000426232.5:c.127A>G | ||
| ENST00000446966.1:c.123A>G | ENSP00000408004.1:p.Pro41= | |
| ENST00000460472.6:c.13283-8945A>G | ENSP00000434586.1:n.13283-8945A>G | |
| ENST00000589042.5:c.39606A>G MANE Select | ENSP00000467141.1:p.Pro13202= | |
| ENST00000591111.5:c.35085A>G | ENSP00000465570.1:p.Pro11695= | |
| ENST00000615779.4:c.35085A>G | ENSP00000483597.1:p.Pro11695= | |
| NM_001256850.1:c.35085A>G | NP_001243779.1:p.Pro11695= | |
| NM_001267550.2:c.39606A>G MANE Select | NP_001254479.2:p.Pro13202= | |
| NM_003319.4:c.13283-8945A>G | NP_003310.4:n.13283-8945A>G | |
| NM_133378.4:c.32304A>G | NP_596869.4:p.Pro10768= | |
| NM_133432.3:c.13658-8945A>G | NP_597676.3:n.13658-8945A>G | |
| NM_133437.4:c.13859-8945A>G | NP_597681.4:n.13859-8945A>G | |
| XM_011511729.1:c.38703A>G | XP_011510031.1:p.Pro12901= | |
| XM_011511730.1:c.13469-8945A>G | XP_011510032.1:n.13469-8945A>G | |
| XM_011511731.1:c.13328-8945A>G | XP_011510033.1:n.13328-8945A>G | |
| XM_017004819.1:c.38499A>G | XP_016860308.1:p.Pro12833= | |
| XM_017004820.1:c.33897A>G | XP_016860309.1:p.Pro11299= | |
| XM_017004821.1:c.33894A>G | XP_016860310.1:p.Pro11298= | |
| XM_017004822.1:c.31859-8945A>G | XP_016860311.1:n.31859-8945A>G | |
| XM_017004823.1:c.13424-8945A>G | XP_016860312.1:n.13424-8945A>G | |
| XM_024453094.1:c.34047A>G | XP_024308862.1:p.Pro11349= | |
| XM_024453095.1:c.34044A>G | XP_024308863.1:p.Pro11348= | |
| XM_024453096.1:c.33477A>G | XP_024308864.1:p.Pro11159= | |
| XM_024453097.1:c.31691-8945A>G | XP_024308865.1:n.31691-8945A>G | |
| XM_024453098.1:c.31610-8945A>G | XP_024308866.1:n.31610-8945A>G | |
| XM_024453099.1:c.13424-8945A>G | XP_024308867.1:n.13424-8945A>G | |
| XM_024453100.1:c.2355A>G | XP_024308868.1:p.Pro785= |