Linked Data
ClinVar Variation Id:
45373
dbSNP Id:
rs397517174
gnomAD v4:
2-39054822-A-G
ERepo:
CA261743/MONDO:0021060/004
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.39054822A>G , CM000664.2:g.39054822A>G | GRCh38 |
| NC_000002.11:g.39281963A>G , CM000664.1:g.39281963A>G | GRCh37 |
| NC_000002.10:g.39135467A>G | NCBI36 |
| NG_007530.1:g.70642T>C , LRG_754:g.70642T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461545.2:n.539T>C | ||
| ENST00000685782.1:n.1350T>C | ||
| ENST00000688189.1:n.277T>C | ||
| ENST00000689668.1:n.519T>C | ||
| ENST00000690679.1:c.612T>C | ||
| ENST00000690876.1:c.512T>C | ENSP00000508955.1:p.Val171Ala | |
| ENST00000691229.1:c.512T>C | ENSP00000510437.1:p.Val171Ala | |
| ENST00000692089.1:c.512T>C | ENSP00000508626.1:p.Val171Ala | |
| ENST00000402219.8:c.512T>C MANE Select | ENSP00000384675.2:p.Val171Ala | |
| ENST00000395038.6:c.512T>C | ENSP00000378479.2:p.Val171Ala | |
| ENST00000402219.6:c.512T>C | ENSP00000384675.2:p.Val171Ala | |
| ENST00000426016.5:c.512T>C | ENSP00000387784.1:p.Val171Ala | |
| NM_005633.3:c.512T>C , LRG_754t1:c.512T>C | NP_005624.2:p.Val171Ala | |
| XM_005264515.3:c.512T>C | XP_005264572.1:p.Val171Ala | |
| XM_011533060.1:c.605T>C | XP_011531362.1:p.Val202Ala | |
| XM_011533061.1:c.605T>C | XP_011531363.1:p.Val202Ala | |
| XM_011533062.1:c.491T>C | XP_011531364.1:p.Val164Ala | |
| XM_011533063.1:c.488T>C | XP_011531365.1:p.Val163Ala | |
| XM_011533064.1:c.341T>C | XP_011531366.1:p.Val114Ala | |
| XM_011533065.1:c.605T>C | XP_011531367.1:p.Val202Ala | |
| XM_005264515.4:c.512T>C | XP_005264572.1:p.Val171Ala | |
| XM_011533062.2:c.491T>C | XP_011531364.1:p.Val164Ala | |
| XM_011533064.2:c.341T>C | XP_011531366.1:p.Val114Ala | |
| NM_001382394.1:c.491T>C | NP_001369323.1:p.Val164Ala | |
| NM_001382395.1:c.512T>C | NP_001369324.1:p.Val171Ala | |
| NM_005633.4:c.512T>C MANE Select | NP_005624.2:p.Val171Ala |