Linked Data
ClinVar Variation Id:
262801
dbSNP Id:
rs2514681
ExAC:
8:101225559 C / G
gnomAD v2:
8-101225559-C-G
gnomAD v3:
8-100213331-C-G
gnomAD v4:
8-100213331-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.100213331C>G , CM000670.2:g.100213331C>G | GRCh38 |
| NC_000008.10:g.101225559C>G , CM000670.1:g.101225559C>G | GRCh37 |
| NC_000008.9:g.101294735C>G | NCBI36 |
| NG_033834.1:g.60297C>G | |
| NG_033834.2:g.60297C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000388798.7:c.1338C>G MANE Select | ENSP00000373450.3:p.Ala446= | |
| ENST00000251809.4:c.1338C>G | ENSP00000251809.3:p.Ala446= | |
| ENST00000388798.6:c.1338C>G | ENSP00000373450.2:p.Ala446= | |
| ENST00000523302.1:n.245C>G | ||
| NM_003114.4:c.1338C>G | NP_003105.2:p.Ala446= | |
| NM_172218.2:c.1338C>G | NP_757367.1:p.Ala446= | |
| XM_011517240.1:c.1338C>G | XP_011515542.1:p.Ala446= | |
| XM_011517241.1:c.1338C>G | XP_011515543.1:p.Ala446= | |
| XM_011517242.1:c.1338C>G | XP_011515544.1:p.Ala446= | |
| XM_011517243.1:c.1338C>G | XP_011515545.1:p.Ala446= | |
| XM_011517244.1:c.1338C>G | XP_011515546.1:p.Ala446= | |
| XM_011517245.1:c.1338C>G | XP_011515547.1:p.Ala446= | |
| XM_011517240.2:c.1338C>G | XP_011515542.1:p.Ala446= | |
| XM_011517241.2:c.1338C>G | XP_011515543.1:p.Ala446= | |
| XM_011517242.2:c.1338C>G | XP_011515544.1:p.Ala446= | |
| XM_011517243.2:c.1338C>G | XP_011515545.1:p.Ala446= | |
| XM_011517245.2:c.1338C>G | XP_011515547.1:p.Ala446= | |
| XM_017013754.1:c.1443C>G | XP_016869243.1:p.Ala481= | |
| XM_017013755.1:c.1002C>G | XP_016869244.1:p.Ala334= | |
| XR_001745580.1:n.1424C>G | ||
| XR_001745581.1:n.1424C>G | ||
| XR_001745582.1:n.1424C>G | ||
| XR_001745583.1:n.1424C>G | ||
| NM_001374321.1:c.1338C>G | NP_001361250.1:p.Ala446= | |
| NM_003114.5:c.1338C>G MANE Select | NP_003105.2:p.Ala446= | |
| NM_172218.3:c.1338C>G | NP_757367.1:p.Ala446= |