Linked Data
ClinVar Variation Id:
193877
dbSNP Id:
rs145447965
ExAC:
2:238275489 T / C
gnomAD v2:
2-238275489-T-C
gnomAD v3:
2-237366846-T-C
gnomAD v4:
2-237366846-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.237366846T>C , CM000664.2:g.237366846T>C | GRCh38 |
| NC_000002.11:g.238275489T>C , CM000664.1:g.238275489T>C | GRCh37 |
| NC_000002.10:g.237940228T>C | NCBI36 |
| NG_008676.1:g.52362A>G , LRG_473:g.52362A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000353578.9:c.4723A>G | ENSP00000315873.4:p.Ile1575Val | |
| ENST00000295550.9:c.5341A>G MANE Select | ENSP00000295550.4:p.Ile1781Val | |
| ENST00000295550.8:c.5341A>G | ENSP00000295550.4:p.Ile1781Val | |
| ENST00000347401.7:c.3520A>G | ENSP00000315609.4:p.Ile1174Val | |
| ENST00000353578.8:c.4723A>G | ENSP00000315873.4:p.Ile1575Val | |
| ENST00000409809.5:c.4723A>G | ENSP00000386844.1:p.Ile1575Val | |
| ENST00000472056.5:c.3520A>G | ENSP00000418285.1:p.Ile1174Val | |
| NM_004369.3:c.5341A>G , LRG_473t1:c.5341A>G | NP_004360.2:p.Ile1781Val | |
| NM_057166.4:c.3520A>G | NP_476507.3:p.Ile1174Val | |
| NM_057167.3:c.4723A>G | NP_476508.2:p.Ile1575Val | |
| XM_005246065.1:c.4741A>G | XP_005246122.1:p.Ile1581Val | |
| XM_005246066.1:c.4120A>G | XP_005246123.1:p.Ile1374Val | |
| XM_006712253.1:c.4840A>G | XP_006712316.1:p.Ile1614Val | |
| XM_011510574.1:c.5338A>G | XP_011508876.1:p.Ile1780Val | |
| XM_011510575.1:c.2935A>G | XP_011508877.1:p.Ile979Val | |
| XM_017003304.1:c.2935A>G | XP_016858793.1:p.Ile979Val | |
| XM_024452684.1:c.4120A>G | XP_024308452.1:p.Ile1374Val | |
| NM_004369.4:c.5341A>G MANE Select | NP_004360.2:p.Ile1781Val | |
| NM_057166.5:c.3520A>G | NP_476507.3:p.Ile1174Val | |
| NM_057167.4:c.4723A>G | NP_476508.2:p.Ile1575Val |