Linked Data
ClinVar Variation Id:
332878
ClinVar RCV Id:
RCV000302696
RCV000301451
RCV000356263
RCV000390517
RCV000391962
RCV000441149
RCV000525321
dbSNP Id:
rs375519815
ExAC:
2:179517222 C / T
gnomAD v2:
2-179517222-C-T
gnomAD v3:
2-178652495-C-T
gnomAD v4:
2-178652495-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178652495C>T , CM000664.2:g.178652495C>T | GRCh38 |
| NC_000002.11:g.179517222C>T , CM000664.1:g.179517222C>T | GRCh37 |
| NC_000002.10:g.179225467C>T | NCBI36 |
| NG_011618.3:g.183308G>A , LRG_391:g.183308G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.31788G>A | ENSP00000343764.6:p.Ala10596= | |
| ENST00000342175.11:c.13859-10178G>A | ENSP00000340554.6:n.13859-10178G>A | |
| ENST00000359218.10:c.13658-10178G>A | ENSP00000352154.5:n.13658-10178G>A | |
| ENST00000342175.10:c.13859-10178G>A | ENSP00000340554.6:n.13859-10178G>A | |
| ENST00000342992.10:c.31788G>A | ENSP00000343764.6:p.Ala10596= | |
| ENST00000359218.9:c.13658-10178G>A | ENSP00000352154.5:n.13658-10178G>A | |
| ENST00000414766.5:c.2441-10178G>A | ENSP00000401501.1:n.2441-10178G>A | |
| ENST00000460472.6:c.13283-10178G>A | ENSP00000434586.1:n.13283-10178G>A | |
| ENST00000589042.5:c.39090G>A MANE Select | ENSP00000467141.1:p.Ala13030= | |
| ENST00000591111.5:c.34569G>A | ENSP00000465570.1:p.Ala11523= | |
| ENST00000615779.4:c.34569G>A | ENSP00000483597.1:p.Ala11523= | |
| NM_001256850.1:c.34569G>A | NP_001243779.1:p.Ala11523= | |
| NM_001267550.2:c.39090G>A MANE Select | NP_001254479.2:p.Ala13030= | |
| NM_003319.4:c.13283-10178G>A | NP_003310.4:n.13283-10178G>A | |
| NM_133378.4:c.31788G>A | NP_596869.4:p.Ala10596= | |
| NM_133432.3:c.13658-10178G>A | NP_597676.3:n.13658-10178G>A | |
| NM_133437.4:c.13859-10178G>A | NP_597681.4:n.13859-10178G>A | |
| XM_011511729.1:c.38187G>A | XP_011510031.1:p.Ala12729= | |
| XM_011511730.1:c.13469-10178G>A | XP_011510032.1:n.13469-10178G>A | |
| XM_011511731.1:c.13328-10178G>A | XP_011510033.1:n.13328-10178G>A | |
| XM_017004819.1:c.37983G>A | XP_016860308.1:p.Ala12661= | |
| XM_017004820.1:c.33381G>A | XP_016860309.1:p.Ala11127= | |
| XM_017004821.1:c.33378G>A | XP_016860310.1:p.Ala11126= | |
| XM_017004822.1:c.31859-10178G>A | XP_016860311.1:n.31859-10178G>A | |
| XM_017004823.1:c.13424-10178G>A | XP_016860312.1:n.13424-10178G>A | |
| XM_024453094.1:c.33569-148G>A | XP_024308862.1:n.33569-148G>A | |
| XM_024453095.1:c.33566-148G>A | XP_024308863.1:n.33566-148G>A | |
| XM_024453096.1:c.32999-148G>A | XP_024308864.1:n.32999-148G>A | |
| XM_024453097.1:c.31691-10178G>A | XP_024308865.1:n.31691-10178G>A | |
| XM_024453098.1:c.31610-10178G>A | XP_024308866.1:n.31610-10178G>A | |
| XM_024453099.1:c.13424-10178G>A | XP_024308867.1:n.13424-10178G>A | |
| XM_024453100.1:c.1839G>A | XP_024308868.1:p.Ala613= |