Linked Data
ClinVar Variation Id:
285190
dbSNP Id:
rs747642083
ExAC:
2:238243493 T / C
gnomAD v2:
2-238243493-T-C
gnomAD v3:
2-237334850-T-C
gnomAD v4:
2-237334850-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.237334850T>C , CM000664.2:g.237334850T>C | GRCh38 |
| NC_000002.11:g.238243493T>C , CM000664.1:g.238243493T>C | GRCh37 |
| NC_000002.10:g.237908232T>C | NCBI36 |
| NG_008676.1:g.84358A>G , LRG_473:g.84358A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000347401.8:c.1610+1285A>G | ||
| ENST00000353578.9:c.8387A>G | ENSP00000315873.4:p.Glu2796Gly | |
| ENST00000682957.1:c.1132A>G | ||
| ENST00000295550.9:c.9005A>G MANE Select | ENSP00000295550.4:p.Glu3002Gly | |
| ENST00000295550.8:c.9005A>G | ENSP00000295550.4:p.Glu3002Gly | |
| ENST00000347401.7:c.7181A>G | ENSP00000315609.4:p.Glu2394Gly | |
| ENST00000353578.8:c.8387A>G | ENSP00000315873.4:p.Glu2796Gly | |
| ENST00000409809.5:c.8387A>G | ENSP00000386844.1:p.Glu2796Gly | |
| ENST00000472056.5:c.7184A>G | ENSP00000418285.1:p.Glu2395Gly | |
| ENST00000491769.1:n.5447A>G | ||
| NM_004369.3:c.9005A>G , LRG_473t1:c.9005A>G | NP_004360.2:p.Glu3002Gly | |
| NM_057166.4:c.7184A>G | NP_476507.3:p.Glu2395Gly | |
| NM_057167.3:c.8387A>G | NP_476508.2:p.Glu2796Gly | |
| XM_005246065.1:c.8405A>G | XP_005246122.1:p.Glu2802Gly | |
| XM_005246066.1:c.7784A>G | XP_005246123.1:p.Glu2595Gly | |
| XM_006712253.1:c.8504A>G | XP_006712316.1:p.Glu2835Gly | |
| XM_011510574.1:c.9002A>G | XP_011508876.1:p.Glu3001Gly | |
| XM_011510575.1:c.6599A>G | XP_011508877.1:p.Glu2200Gly | |
| XM_017003304.1:c.6599A>G | XP_016858793.1:p.Glu2200Gly | |
| XM_024452684.1:c.7784A>G | XP_024308452.1:p.Glu2595Gly | |
| NM_004369.4:c.9005A>G MANE Select | NP_004360.2:p.Glu3002Gly | |
| NM_057166.5:c.7184A>G | NP_476507.3:p.Glu2395Gly | |
| NM_057167.4:c.8387A>G | NP_476508.2:p.Glu2796Gly |