Linked Data
ClinVar Variation Id:
1535147
ClinVar RCV Id:
RCV002089972
dbSNP Id:
rs1017213900
gnomAD v4:
13-23340486-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23340486G>A , CM000675.2:g.23340486G>A | GRCh38 |
| NC_000013.10:g.23914625G>A , CM000675.1:g.23914625G>A | GRCh37 |
| NC_000013.9:g.22812625G>A | NCBI36 |
| NG_012342.1:g.98217C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682775.1:c.2185+13299C>T | ENSP00000508399.1:n.2185+13299C>T | |
| ENST00000682944.1:c.3417C>T | ENSP00000507173.1:p.Thr1139= | |
| ENST00000683210.1:c.2185+13299C>T | ENSP00000506739.1:n.2185+13299C>T | |
| ENST00000683270.1:c.3381C>T | ENSP00000507624.1:p.Thr1127= | |
| ENST00000683367.1:c.2177-11002C>T | ENSP00000507780.1:n.2177-11002C>T | |
| ENST00000683489.1:c.2291+1099C>T | ENSP00000508403.1:n.2291+1099C>T | |
| ENST00000683680.1:c.2318+1099C>T | ENSP00000507223.1:n.2318+1099C>T | |
| ENST00000684163.1:c.2203+6325C>T | ENSP00000508262.1:n.2203+6325C>T | |
| ENST00000684196.1:n.4543-11002C>T | ||
| ENST00000684325.1:c.2185+13299C>T | ENSP00000508121.1:n.2185+13299C>T | |
| ENST00000684385.1:c.2220+6325C>T | ENSP00000507855.1:n.2220+6325C>T | |
| ENST00000684497.1:c.2185+13299C>T | ENSP00000507057.1:n.2185+13299C>T | |
| ENST00000382292.9:c.3390C>T MANE Select | ENSP00000371729.3:p.Thr1130= | |
| ENST00000423156.2:c.2186-11002C>T | ENSP00000390925.2:n.2186-11002C>T | |
| ENST00000455470.6:c.2431+959C>T | ENSP00000406565.2:n.2431+959C>T | |
| ENST00000382292.7:c.3390C>T | ENSP00000371729.3:p.Thr1130= | |
| ENST00000382298.7:c.3390C>T | ENSP00000371735.3:p.Thr1130= | |
| ENST00000402364.1:c.1140C>T | ENSP00000385844.1:p.Thr380= | |
| ENST00000423156.1:c.1058-11002C>T | ENSP00000390925.1:n.1058-11002C>T | |
| ENST00000455470.5:c.2129+959C>T | ||
| NM_001278055.1:c.2949C>T | NP_001264984.1:p.Thr983= | |
| NM_014363.5:c.3390C>T | NP_055178.3:p.Thr1130= | |
| XM_005266338.1:c.3417C>T | XP_005266395.1:p.Thr1139= | |
| XM_011535038.1:c.3441C>T | XP_011533340.1:p.Thr1147= | |
| XM_011535039.1:c.3408C>T | XP_011533341.1:p.Thr1136= | |
| XM_005266338.2:c.3417C>T | XP_005266395.1:p.Thr1139= | |
| XM_011535039.2:c.3408C>T | XP_011533341.1:p.Thr1136= | |
| XM_017020539.1:c.3381C>T | XP_016876028.1:p.Thr1127= | |
| XM_024449337.1:c.3417C>T | XP_024305105.1:p.Thr1139= | |
| NM_014363.6:c.3390C>T MANE Select | NP_055178.3:p.Thr1130= | |
| NM_001278055.2:c.2949C>T | NP_001264984.1:p.Thr983= |