Linked Data
ClinVar Variation Id:
960350
dbSNP Id:
rs757286231
ExAC:
2:167159728 A / C
gnomAD v2:
2-167159728-A-C
gnomAD v3:
2-166303218-A-C
gnomAD v4:
2-166303218-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.166303218A>C , CM000664.2:g.166303218A>C | GRCh38 |
| NC_000002.11:g.167159728A>C , CM000664.1:g.167159728A>C | GRCh37 |
| NC_000002.10:g.166867974A>C | NCBI36 |
| NG_012798.1:g.77770T>G , LRG_369:g.77770T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303354.11:c.773T>G | ENSP00000304748.7:p.Val258Gly | |
| ENST00000409435.6:c.773T>G | ENSP00000386330.2:p.Val258Gly | |
| ENST00000452182.2:c.773T>G | ENSP00000393141.2:p.Val258Gly | |
| ENST00000454569.6:c.773T>G | ENSP00000413212.2:p.Val258Gly | |
| ENST00000472119.2:n.1128T>G | ||
| ENST00000642356.2:c.773T>G MANE Select | ENSP00000495601.1:p.Val258Gly | |
| ENST00000644316.1:c.773T>G | ENSP00000493939.1:p.Val258Gly | |
| ENST00000645815.1:n.144T>G | ||
| ENST00000645907.1:c.773T>G | ENSP00000495983.1:p.Val258Gly | |
| ENST00000303354.10:c.773T>G | ENSP00000304748.7:p.Val258Gly | |
| ENST00000409435.5:c.773T>G | ENSP00000386330.1:p.Val258Gly | |
| ENST00000409672.5:c.773T>G | ENSP00000386306.1:p.Val258Gly | |
| ENST00000452182.1:c.368T>G | ENSP00000393141.1:p.Val123Gly | |
| ENST00000454569.5:c.368T>G | ENSP00000413212.1:p.Val123Gly | |
| ENST00000472119.1:n.306T>G | ||
| NM_002977.3:c.773T>G , LRG_369t1:c.773T>G | NP_002968.1:p.Val258Gly | |
| XM_005246757.1:c.773T>G | XP_005246814.1:p.Val258Gly | |
| XM_011511616.1:c.773T>G | XP_011509918.1:p.Val258Gly | |
| XM_011511617.1:c.773T>G | XP_011509919.1:p.Val258Gly | |
| XM_011511618.1:c.773T>G | XP_011509920.1:p.Val258Gly | |
| XM_011511619.1:c.773T>G | XP_011509921.1:p.Val258Gly | |
| NM_001365536.1:c.773T>G MANE Select | NP_001352465.1:p.Val258Gly | |
| XM_011511616.3:c.773T>G | XP_011509918.1:p.Val258Gly | |
| XM_011511617.2:c.773T>G | XP_011509919.1:p.Val258Gly | |
| XM_011511618.2:c.773T>G | XP_011509920.1:p.Val258Gly | |
| XM_011511619.2:c.773T>G | XP_011509921.1:p.Val258Gly | |
| XM_017004668.1:c.386T>G | XP_016860157.1:p.Val129Gly | |
| XM_017004669.1:c.29T>G | XP_016860158.1:p.Val10Gly | |
| XR_001738886.1:n.1087T>G |