Linked Data
ClinVar Variation Id:
1094410
ClinVar RCV Id:
RCV001414933
dbSNP Id:
rs148209022
ExAC:
13:23910041 G / C
gnomAD v2:
13-23910041-G-C
gnomAD v3:
13-23335902-G-C
gnomAD v4:
13-23335902-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23335902G>C , CM000675.2:g.23335902G>C | GRCh38 |
| NC_000013.10:g.23910041G>C , CM000675.1:g.23910041G>C | GRCh37 |
| NC_000013.9:g.22808041G>C | NCBI36 |
| NG_012342.1:g.102801C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682775.1:c.2185+17883C>G | ENSP00000508399.1:n.2185+17883C>G | |
| ENST00000682944.1:c.8001C>G | ENSP00000507173.1:p.Ala2667= | |
| ENST00000683210.1:c.2185+17883C>G | ENSP00000506739.1:n.2185+17883C>G | |
| ENST00000683270.1:c.6445+1520C>G | ENSP00000507624.1:n.6445+1520C>G | |
| ENST00000683367.1:c.2177-6418C>G | ENSP00000507780.1:n.2177-6418C>G | |
| ENST00000683489.1:c.2291+5683C>G | ENSP00000508403.1:n.2291+5683C>G | |
| ENST00000683680.1:c.2318+5683C>G | ENSP00000507223.1:n.2318+5683C>G | |
| ENST00000684163.1:c.2204-6418C>G | ENSP00000508262.1:n.2204-6418C>G | |
| ENST00000684196.1:n.4543-6418C>G | ||
| ENST00000684325.1:c.2186-14228C>G | ENSP00000508121.1:n.2186-14228C>G | |
| ENST00000684385.1:c.2221-6418C>G | ENSP00000507855.1:n.2221-6418C>G | |
| ENST00000684497.1:c.2186-13258C>G | ENSP00000507057.1:n.2186-13258C>G | |
| ENST00000382292.9:c.7974C>G MANE Select | ENSP00000371729.3:p.Ala2658= | |
| ENST00000423156.2:c.2186-6418C>G | ENSP00000390925.2:n.2186-6418C>G | |
| ENST00000455470.6:c.2431+5543C>G | ENSP00000406565.2:n.2431+5543C>G | |
| ENST00000382292.7:c.7974C>G | ENSP00000371729.3:p.Ala2658= | |
| ENST00000382298.7:c.7974C>G | ENSP00000371735.3:p.Ala2658= | |
| ENST00000402364.1:c.5724C>G | ENSP00000385844.1:p.Ala1908= | |
| ENST00000423156.1:c.1058-6418C>G | ENSP00000390925.1:n.1058-6418C>G | |
| ENST00000455470.5:c.2129+5543C>G | ||
| NM_001278055.1:c.7533C>G | NP_001264984.1:p.Ala2511= | |
| NM_014363.5:c.7974C>G | NP_055178.3:p.Ala2658= | |
| XM_005266338.1:c.8001C>G | XP_005266395.1:p.Ala2667= | |
| XM_011535038.1:c.8025C>G | XP_011533340.1:p.Ala2675= | |
| XM_011535039.1:c.7992C>G | XP_011533341.1:p.Ala2664= | |
| XM_005266338.2:c.8001C>G | XP_005266395.1:p.Ala2667= | |
| XM_011535039.2:c.7992C>G | XP_011533341.1:p.Ala2664= | |
| XM_017020539.1:c.7965C>G | XP_016876028.1:p.Ala2655= | |
| XM_024449337.1:c.8001C>G | XP_024305105.1:p.Ala2667= | |
| NM_014363.6:c.7974C>G MANE Select | NP_055178.3:p.Ala2658= | |
| NM_001278055.2:c.7533C>G | NP_001264984.1:p.Ala2511= |