Linked Data
ClinVar Variation Id:
497592
dbSNP Id:
rs765101399
ExAC:
2:238243300 G / A
gnomAD v2:
2-238243300-G-A
gnomAD v3:
2-237334657-G-A
gnomAD v4:
2-237334657-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.237334657G>A , CM000664.2:g.237334657G>A | GRCh38 |
| NC_000002.11:g.238243300G>A , CM000664.1:g.238243300G>A | GRCh37 |
| NC_000002.10:g.237908039G>A | NCBI36 |
| NG_008676.1:g.84551C>T , LRG_473:g.84551C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000347401.8:c.1611-1109C>T | ||
| ENST00000353578.9:c.8580C>T | ENSP00000315873.4:p.Val2860= | |
| ENST00000682957.1:c.1325C>T | ||
| ENST00000683348.1:c.66C>T | ENSP00000508058.1:p.Val22= | |
| ENST00000295550.9:c.9198C>T MANE Select | ENSP00000295550.4:p.Val3066= | |
| ENST00000295550.8:c.9198C>T | ENSP00000295550.4:p.Val3066= | |
| ENST00000347401.7:c.7374C>T | ENSP00000315609.4:p.Val2458= | |
| ENST00000353578.8:c.8580C>T | ENSP00000315873.4:p.Val2860= | |
| ENST00000409809.5:c.8580C>T | ENSP00000386844.1:p.Val2860= | |
| ENST00000472056.5:c.7377C>T | ENSP00000418285.1:p.Val2459= | |
| ENST00000491769.1:n.5640C>T | ||
| ENST00000493608.1:n.130C>T | ||
| NM_004369.3:c.9198C>T , LRG_473t1:c.9198C>T | NP_004360.2:p.Val3066= | |
| NM_057166.4:c.7377C>T | NP_476507.3:p.Val2459= | |
| NM_057167.3:c.8580C>T | NP_476508.2:p.Val2860= | |
| XM_005246065.1:c.8598C>T | XP_005246122.1:p.Val2866= | |
| XM_005246066.1:c.7977C>T | XP_005246123.1:p.Val2659= | |
| XM_006712253.1:c.8697C>T | XP_006712316.1:p.Val2899= | |
| XM_011510574.1:c.9195C>T | XP_011508876.1:p.Val3065= | |
| XM_011510575.1:c.6792C>T | XP_011508877.1:p.Val2264= | |
| XM_017003304.1:c.6792C>T | XP_016858793.1:p.Val2264= | |
| XM_024452684.1:c.7977C>T | XP_024308452.1:p.Val2659= | |
| NM_004369.4:c.9198C>T MANE Select | NP_004360.2:p.Val3066= | |
| NM_057166.5:c.7377C>T | NP_476507.3:p.Val2459= | |
| NM_057167.4:c.8580C>T | NP_476508.2:p.Val2860= |