Linked Data
ClinVar Variation Id:
1196599
ClinVar RCV Id:
RCV001560119
dbSNP Id:
rs116246188
gnomAD v2:
13-23932833-T-C
gnomAD v3:
13-23358694-T-C
gnomAD v4:
13-23358694-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23358694T>C , CM000675.2:g.23358694T>C | GRCh38 |
| NC_000013.10:g.23932833T>C , CM000675.1:g.23932833T>C | GRCh37 |
| NC_000013.9:g.22830833T>C | NCBI36 |
| NG_012342.1:g.80009A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682775.1:c.458-213A>G | ENSP00000508399.1:n.458-213A>G | |
| ENST00000682944.1:c.458-213A>G | ENSP00000507173.1:n.458-213A>G | |
| ENST00000683154.1:n.596-213A>G | ||
| ENST00000683210.1:c.458-213A>G | ENSP00000506739.1:n.458-213A>G | |
| ENST00000683270.1:c.449-213A>G | ENSP00000507624.1:n.449-213A>G | |
| ENST00000683367.1:c.449-213A>G | ENSP00000507780.1:n.449-213A>G | |
| ENST00000683489.1:c.458-213A>G | ENSP00000508403.1:n.458-213A>G | |
| ENST00000683680.1:c.458-213A>G | ENSP00000507223.1:n.458-213A>G | |
| ENST00000684163.1:c.449-213A>G | ENSP00000508262.1:n.449-213A>G | |
| ENST00000684196.1:n.2815-213A>G | ||
| ENST00000684325.1:c.458-213A>G | ENSP00000508121.1:n.458-213A>G | |
| ENST00000684385.1:c.458-213A>G | ENSP00000507855.1:n.458-213A>G | |
| ENST00000684497.1:c.458-213A>G | ENSP00000507057.1:n.458-213A>G | |
| ENST00000382292.9:c.458-213A>G MANE Select | ENSP00000371729.3:n.458-213A>G | |
| ENST00000423156.2:c.458-213A>G | ENSP00000390925.2:n.458-213A>G | |
| ENST00000455470.6:c.458-213A>G | ENSP00000406565.2:n.458-213A>G | |
| ENST00000382292.7:c.458-213A>G | ENSP00000371729.3:n.458-213A>G | |
| ENST00000382298.7:c.458-213A>G | ENSP00000371735.3:n.458-213A>G | |
| ENST00000402364.1:c.-1793-213A>G | ENSP00000385844.1:n.-1793-213A>G | |
| ENST00000455470.5:c.156-213A>G | ||
| NM_001278055.1:c.17-213A>G | NP_001264984.1:n.17-213A>G | |
| NM_014363.5:c.458-213A>G | NP_055178.3:n.458-213A>G | |
| XM_005266338.1:c.458-213A>G | XP_005266395.1:n.458-213A>G | |
| XM_011535038.1:c.482-213A>G | XP_011533340.1:n.482-213A>G | |
| XM_011535039.1:c.449-213A>G | XP_011533341.1:n.449-213A>G | |
| XM_005266338.2:c.458-213A>G | XP_005266395.1:n.458-213A>G | |
| XM_011535039.2:c.449-213A>G | XP_011533341.1:n.449-213A>G | |
| XM_017020539.1:c.449-213A>G | XP_016876028.1:n.449-213A>G | |
| XM_024449337.1:c.458-213A>G | XP_024305105.1:n.458-213A>G | |
| NM_014363.6:c.458-213A>G MANE Select | NP_055178.3:n.458-213A>G | |
| NM_001278055.2:c.17-213A>G | NP_001264984.1:n.17-213A>G |