Linked Data
ClinVar Variation Id:
311501
dbSNP Id:
rs150959878
ExAC:
13:23905577 C / T
gnomAD v2:
13-23905577-C-T
gnomAD v3:
13-23331438-C-T
gnomAD v4:
13-23331438-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23331438C>T , CM000675.2:g.23331438C>T | GRCh38 |
| NC_000013.10:g.23905577C>T , CM000675.1:g.23905577C>T | GRCh37 |
| NC_000013.9:g.22803577C>T | NCBI36 |
| NG_012342.1:g.107265G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682775.1:c.2186-19323G>A | ENSP00000508399.1:n.2186-19323G>A | |
| ENST00000682944.1:c.12465G>A | ENSP00000507173.1:p.Ser4155= | |
| ENST00000683210.1:c.2185+22347G>A | ENSP00000506739.1:n.2185+22347G>A | |
| ENST00000683270.1:c.6446-1954G>A | ENSP00000507624.1:n.6446-1954G>A | |
| ENST00000683367.1:c.2177-1954G>A | ENSP00000507780.1:n.2177-1954G>A | |
| ENST00000683489.1:c.2292-1486G>A | ENSP00000508403.1:n.2292-1486G>A | |
| ENST00000683680.1:c.2319-1486G>A | ENSP00000507223.1:n.2319-1486G>A | |
| ENST00000684163.1:c.2204-1954G>A | ENSP00000508262.1:n.2204-1954G>A | |
| ENST00000684196.1:n.4543-1954G>A | ||
| ENST00000684325.1:c.2186-9764G>A | ENSP00000508121.1:n.2186-9764G>A | |
| ENST00000684385.1:c.2221-1954G>A | ENSP00000507855.1:n.2221-1954G>A | |
| ENST00000684497.1:c.2186-8794G>A | ENSP00000507057.1:n.2186-8794G>A | |
| ENST00000382292.9:c.12438G>A MANE Select | ENSP00000371729.3:p.Ser4146= | |
| ENST00000423156.2:c.2186-1954G>A | ENSP00000390925.2:n.2186-1954G>A | |
| ENST00000455470.6:c.2432-1954G>A | ENSP00000406565.2:n.2432-1954G>A | |
| ENST00000382292.7:c.12438G>A | ENSP00000371729.3:p.Ser4146= | |
| ENST00000382298.7:c.12438G>A | ENSP00000371735.3:p.Ser4146= | |
| ENST00000402364.1:c.10188G>A | ENSP00000385844.1:p.Ser3396= | |
| ENST00000423156.1:c.1058-1954G>A | ENSP00000390925.1:n.1058-1954G>A | |
| ENST00000455470.5:c.2130-1954G>A | ||
| NM_001278055.1:c.11997G>A | NP_001264984.1:p.Ser3999= | |
| NM_014363.5:c.12438G>A | NP_055178.3:p.Ser4146= | |
| XM_005266338.1:c.12465G>A | XP_005266395.1:p.Ser4155= | |
| XM_011535038.1:c.12489G>A | XP_011533340.1:p.Ser4163= | |
| XM_011535039.1:c.12456G>A | XP_011533341.1:p.Ser4152= | |
| XM_005266338.2:c.12465G>A | XP_005266395.1:p.Ser4155= | |
| XM_011535039.2:c.12456G>A | XP_011533341.1:p.Ser4152= | |
| XM_017020539.1:c.12429G>A | XP_016876028.1:p.Ser4143= | |
| XM_024449337.1:c.12465G>A | XP_024305105.1:p.Ser4155= | |
| NM_014363.6:c.12438G>A MANE Select | NP_055178.3:p.Ser4146= | |
| NM_001278055.2:c.11997G>A | NP_001264984.1:p.Ser3999= |