Linked Data
ClinVar Variation Id:
701329
dbSNP Id:
rs780674369
ExAC:
13:23905409 T / G
gnomAD v2:
13-23905409-T-G
gnomAD v3:
13-23331270-T-G
gnomAD v4:
13-23331270-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23331270T>G , CM000675.2:g.23331270T>G | GRCh38 |
| NC_000013.10:g.23905409T>G , CM000675.1:g.23905409T>G | GRCh37 |
| NC_000013.9:g.22803409T>G | NCBI36 |
| NG_012342.1:g.107433A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682775.1:c.2186-19155A>C | ENSP00000508399.1:n.2186-19155A>C | |
| ENST00000682944.1:c.12633A>C | ENSP00000507173.1:p.Thr4211= | |
| ENST00000683210.1:c.2185+22515A>C | ENSP00000506739.1:n.2185+22515A>C | |
| ENST00000683270.1:c.6446-1786A>C | ENSP00000507624.1:n.6446-1786A>C | |
| ENST00000683367.1:c.2177-1786A>C | ENSP00000507780.1:n.2177-1786A>C | |
| ENST00000683489.1:c.2292-1318A>C | ENSP00000508403.1:n.2292-1318A>C | |
| ENST00000683680.1:c.2319-1318A>C | ENSP00000507223.1:n.2319-1318A>C | |
| ENST00000684163.1:c.2204-1786A>C | ENSP00000508262.1:n.2204-1786A>C | |
| ENST00000684196.1:n.4543-1786A>C | ||
| ENST00000684325.1:c.2186-9596A>C | ENSP00000508121.1:n.2186-9596A>C | |
| ENST00000684385.1:c.2221-1786A>C | ENSP00000507855.1:n.2221-1786A>C | |
| ENST00000684497.1:c.2186-8626A>C | ENSP00000507057.1:n.2186-8626A>C | |
| ENST00000382292.9:c.12606A>C MANE Select | ENSP00000371729.3:p.Thr4202= | |
| ENST00000423156.2:c.2186-1786A>C | ENSP00000390925.2:n.2186-1786A>C | |
| ENST00000455470.6:c.2432-1786A>C | ENSP00000406565.2:n.2432-1786A>C | |
| ENST00000382292.7:c.12606A>C | ENSP00000371729.3:p.Thr4202= | |
| ENST00000382298.7:c.12606A>C | ENSP00000371735.3:p.Thr4202= | |
| ENST00000402364.1:c.10356A>C | ENSP00000385844.1:p.Thr3452= | |
| ENST00000423156.1:c.1058-1786A>C | ENSP00000390925.1:n.1058-1786A>C | |
| ENST00000455470.5:c.2130-1786A>C | ||
| NM_001278055.1:c.12165A>C | NP_001264984.1:p.Thr4055= | |
| NM_014363.5:c.12606A>C | NP_055178.3:p.Thr4202= | |
| XM_005266338.1:c.12633A>C | XP_005266395.1:p.Thr4211= | |
| XM_011535038.1:c.12657A>C | XP_011533340.1:p.Thr4219= | |
| XM_011535039.1:c.12624A>C | XP_011533341.1:p.Thr4208= | |
| XM_005266338.2:c.12633A>C | XP_005266395.1:p.Thr4211= | |
| XM_011535039.2:c.12624A>C | XP_011533341.1:p.Thr4208= | |
| XM_017020539.1:c.12597A>C | XP_016876028.1:p.Thr4199= | |
| XM_024449337.1:c.12633A>C | XP_024305105.1:p.Thr4211= | |
| NM_014363.6:c.12606A>C MANE Select | NP_055178.3:p.Thr4202= | |
| NM_001278055.2:c.12165A>C | NP_001264984.1:p.Thr4055= |