Linked Data
ClinVar Variation Id:
130199
dbSNP Id:
rs17078605
ExAC:
13:23907909 A / G
gnomAD v2:
13-23907909-A-G
gnomAD v3:
13-23333770-A-G
gnomAD v4:
13-23333770-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23333770A>G , CM000675.2:g.23333770A>G | GRCh38 |
| NC_000013.10:g.23907909A>G , CM000675.1:g.23907909A>G | GRCh37 |
| NC_000013.9:g.22805909A>G | NCBI36 |
| NG_012342.1:g.104933T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682775.1:c.2185+20015T>C | ENSP00000508399.1:n.2185+20015T>C | |
| ENST00000682944.1:c.10133T>C | ENSP00000507173.1:p.Val3378Ala | |
| ENST00000683210.1:c.2185+20015T>C | ENSP00000506739.1:n.2185+20015T>C | |
| ENST00000683270.1:c.6445+3652T>C | ENSP00000507624.1:n.6445+3652T>C | |
| ENST00000683367.1:c.2177-4286T>C | ENSP00000507780.1:n.2177-4286T>C | |
| ENST00000683489.1:c.2292-3818T>C | ENSP00000508403.1:n.2292-3818T>C | |
| ENST00000683680.1:c.2319-3818T>C | ENSP00000507223.1:n.2319-3818T>C | |
| ENST00000684163.1:c.2204-4286T>C | ENSP00000508262.1:n.2204-4286T>C | |
| ENST00000684196.1:n.4543-4286T>C | ||
| ENST00000684325.1:c.2186-12096T>C | ENSP00000508121.1:n.2186-12096T>C | |
| ENST00000684385.1:c.2221-4286T>C | ENSP00000507855.1:n.2221-4286T>C | |
| ENST00000684497.1:c.2186-11126T>C | ENSP00000507057.1:n.2186-11126T>C | |
| ENST00000382292.9:c.10106T>C MANE Select | ENSP00000371729.3:p.Val3369Ala | |
| ENST00000423156.2:c.2186-4286T>C | ENSP00000390925.2:n.2186-4286T>C | |
| ENST00000455470.6:c.2432-4286T>C | ENSP00000406565.2:n.2432-4286T>C | |
| ENST00000382292.7:c.10106T>C | ENSP00000371729.3:p.Val3369Ala | |
| ENST00000382298.7:c.10106T>C | ENSP00000371735.3:p.Val3369Ala | |
| ENST00000402364.1:c.7856T>C | ENSP00000385844.1:p.Val2619Ala | |
| ENST00000423156.1:c.1058-4286T>C | ENSP00000390925.1:n.1058-4286T>C | |
| ENST00000455470.5:c.2130-4286T>C | ||
| NM_001278055.1:c.9665T>C | NP_001264984.1:p.Val3222Ala | |
| NM_014363.5:c.10106T>C | NP_055178.3:p.Val3369Ala | |
| XM_005266338.1:c.10133T>C | XP_005266395.1:p.Val3378Ala | |
| XM_011535038.1:c.10157T>C | XP_011533340.1:p.Val3386Ala | |
| XM_011535039.1:c.10124T>C | XP_011533341.1:p.Val3375Ala | |
| XM_005266338.2:c.10133T>C | XP_005266395.1:p.Val3378Ala | |
| XM_011535039.2:c.10124T>C | XP_011533341.1:p.Val3375Ala | |
| XM_017020539.1:c.10097T>C | XP_016876028.1:p.Val3366Ala | |
| XM_024449337.1:c.10133T>C | XP_024305105.1:p.Val3378Ala | |
| NM_014363.6:c.10106T>C MANE Select | NP_055178.3:p.Val3369Ala | |
| NM_001278055.2:c.9665T>C | NP_001264984.1:p.Val3222Ala |