Linked Data
ClinVar Variation Id:
1140435
ClinVar RCV Id:
RCV001477505
dbSNP Id:
rs201862823
gnomAD v3:
12-6333425-T-C
gnomAD v4:
12-6333425-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6333425T>C , CM000674.2:g.6333425T>C | GRCh38 |
| NC_000012.11:g.6442591T>C , CM000674.1:g.6442591T>C | GRCh37 |
| NC_000012.10:g.6312852T>C | NCBI36 |
| NG_007506.1:g.13671A>G , LRG_193:g.13671A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366159.9:n.448A>G | ||
| ENST00000437813.8:c.414A>G | ENSP00000513672.1:p.Glu138= | |
| ENST00000440083.7:c.414A>G | ENSP00000413224.3:p.Glu138= | |
| ENST00000535958.2:c.*241A>G | ENSP00000513673.1:n.*241A>G | |
| ENST00000698339.1:c.414A>G | ENSP00000513670.1:p.Glu138= | |
| ENST00000698340.1:c.414A>G | ENSP00000513671.1:p.Glu138= | |
| ENST00000162749.7:c.414A>G MANE Select | ENSP00000162749.2:p.Glu138= | |
| ENST00000162749.6:c.414A>G | ENSP00000162749.2:p.Glu138= | |
| ENST00000366159.8:c.414A>G | ENSP00000380389.3:p.Glu138= | |
| ENST00000437813.7:n.375A>G | ||
| ENST00000440083.6:c.414A>G | ENSP00000413224.2:p.Glu138= | |
| ENST00000534885.5:c.260A>G | ENSP00000441803.1:p.Lys87Arg | |
| ENST00000537842.5:n.18A>G | ||
| ENST00000539372.5:c.414A>G | ENSP00000442059.1:p.Glu138= | |
| ENST00000540022.5:c.285A>G | ENSP00000438343.1:p.Glu95= | |
| ENST00000543048.5:c.*25A>G | ENSP00000439981.1:n.*25A>G | |
| ENST00000543995.5:c.*1A>G | ENSP00000442405.1:n.*1A>G | |
| NM_001065.3:c.414A>G , LRG_193t1:c.414A>G | NP_001056.1:p.Glu138= | |
| NM_001346091.1:c.90A>G | NP_001333020.1:p.Glu30= | |
| NM_001346092.1:c.-164A>G | NP_001333021.1:n.-164A>G | |
| NR_144351.1:n.717A>G | ||
| NM_001065.4:c.414A>G MANE Select | NP_001056.1:p.Glu138= | |
| NM_001346091.2:c.90A>G | NP_001333020.1:p.Glu30= | |
| NM_001346092.2:c.-164A>G | NP_001333021.1:n.-164A>G | |
| NR_144351.2:n.676A>G |