Linked Data
ClinVar Variation Id:
2736008
ClinVar RCV Id:
RCV003530949
dbSNP Id:
rs431825362
gnomAD v4:
13-32363187-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32363187C>G , CM000675.2:g.32363187C>G | GRCh38 |
| NC_000013.10:g.32937324C>G , CM000675.1:g.32937324C>G | GRCh37 |
| NC_000013.9:g.31835324C>G | NCBI36 |
| NG_012772.3:g.52708C>G , LRG_293:g.52708C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.7985C>G | ENSP00000434898.2:p.Thr2662Arg | |
| ENST00000528762.2:c.7985C>G | ENSP00000433168.2:p.Thr2662Arg | |
| ENST00000530893.7:c.7616C>G | ENSP00000499438.2:p.Thr2539Arg | |
| ENST00000665585.2:c.7985C>G | ENSP00000499570.2:p.Thr2662Arg | |
| ENST00000666593.2:c.7985C>G | ENSP00000499256.2:p.Thr2662Arg | |
| ENST00000700202.2:c.7985C>G | ENSP00000514856.2:p.Thr2662Arg | |
| ENST00000700202.1:c.452C>G | ENSP00000514856.1:p.Thr151Arg | |
| ENST00000380152.8:c.7985C>G MANE Select | ENSP00000369497.3:p.Thr2662Arg | |
| ENST00000544455.6:c.7985C>G | ENSP00000439902.1:p.Thr2662Arg | |
| ENST00000614259.2:c.7993C>G | ENSP00000506251.1:n.7993C>G | |
| ENST00000665585.1:c.550C>G | ||
| ENST00000680887.1:c.7985C>G | ENSP00000505508.1:p.Thr2662Arg | |
| ENST00000380152.7:c.7985C>G | ENSP00000369497.3:p.Thr2662Arg | |
| ENST00000544455.5:c.7985C>G | ENSP00000439902.1:p.Thr2662Arg | |
| NM_000059.3:c.7985C>G , LRG_293t1:c.7985C>G | NP_000050.2:p.Thr2662Arg | |
| XM_011535203.1:c.7985C>G | XP_011533505.1:p.Thr2662Arg | |
| XM_011535204.1:c.7889C>G | XP_011533506.1:p.Thr2630Arg | |
| XM_011535205.1:c.7985C>G | XP_011533507.1:p.Thr2662Arg | |
| NM_000059.4:c.7985C>G MANE Select | NP_000050.3:p.Thr2662Arg |