Linked Data
dbSNP Id:
rs770368952
ExAC:
13:23905329 A / T
gnomAD v2:
13-23905329-A-T
gnomAD v3:
13-23331190-A-T
gnomAD v4:
13-23331190-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23331190A>T , CM000675.2:g.23331190A>T | GRCh38 |
| NC_000013.10:g.23905329A>T , CM000675.1:g.23905329A>T | GRCh37 |
| NC_000013.9:g.22803329A>T | NCBI36 |
| NG_012342.1:g.107513T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682775.1:c.2186-19075T>A | ENSP00000508399.1:n.2186-19075T>A | |
| ENST00000682944.1:c.12713T>A | ENSP00000507173.1:p.Ile4238Asn | |
| ENST00000683210.1:c.2185+22595T>A | ENSP00000506739.1:n.2185+22595T>A | |
| ENST00000683270.1:c.6446-1706T>A | ENSP00000507624.1:n.6446-1706T>A | |
| ENST00000683367.1:c.2177-1706T>A | ENSP00000507780.1:n.2177-1706T>A | |
| ENST00000683489.1:c.2292-1238T>A | ENSP00000508403.1:n.2292-1238T>A | |
| ENST00000683680.1:c.2319-1238T>A | ENSP00000507223.1:n.2319-1238T>A | |
| ENST00000684163.1:c.2204-1706T>A | ENSP00000508262.1:n.2204-1706T>A | |
| ENST00000684196.1:n.4543-1706T>A | ||
| ENST00000684325.1:c.2186-9516T>A | ENSP00000508121.1:n.2186-9516T>A | |
| ENST00000684385.1:c.2221-1706T>A | ENSP00000507855.1:n.2221-1706T>A | |
| ENST00000684497.1:c.2186-8546T>A | ENSP00000507057.1:n.2186-8546T>A | |
| ENST00000382292.9:c.12686T>A MANE Select | ENSP00000371729.3:p.Ile4229Asn | |
| ENST00000423156.2:c.2186-1706T>A | ENSP00000390925.2:n.2186-1706T>A | |
| ENST00000455470.6:c.2432-1706T>A | ENSP00000406565.2:n.2432-1706T>A | |
| ENST00000382292.7:c.12686T>A | ENSP00000371729.3:p.Ile4229Asn | |
| ENST00000382298.7:c.12686T>A | ENSP00000371735.3:p.Ile4229Asn | |
| ENST00000402364.1:c.10436T>A | ENSP00000385844.1:p.Ile3479Asn | |
| ENST00000423156.1:c.1058-1706T>A | ENSP00000390925.1:n.1058-1706T>A | |
| ENST00000455470.5:c.2130-1706T>A | ||
| NM_001278055.1:c.12245T>A | NP_001264984.1:p.Ile4082Asn | |
| NM_014363.5:c.12686T>A | NP_055178.3:p.Ile4229Asn | |
| XM_005266338.1:c.12713T>A | XP_005266395.1:p.Ile4238Asn | |
| XM_011535038.1:c.12737T>A | XP_011533340.1:p.Ile4246Asn | |
| XM_011535039.1:c.12704T>A | XP_011533341.1:p.Ile4235Asn | |
| XM_005266338.2:c.12713T>A | XP_005266395.1:p.Ile4238Asn | |
| XM_011535039.2:c.12704T>A | XP_011533341.1:p.Ile4235Asn | |
| XM_017020539.1:c.12677T>A | XP_016876028.1:p.Ile4226Asn | |
| XM_024449337.1:c.12713T>A | XP_024305105.1:p.Ile4238Asn | |
| NM_014363.6:c.12686T>A MANE Select | NP_055178.3:p.Ile4229Asn | |
| NM_001278055.2:c.12245T>A | NP_001264984.1:p.Ile4082Asn |