Linked Data
ClinVar Variation Id:
236822
dbSNP Id:
rs780472557
ExAC:
15:91292949 A / G
gnomAD v2:
15-91292949-A-G
gnomAD v3:
15-90749719-A-G
gnomAD v4:
15-90749719-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.90749719A>G , CM000677.2:g.90749719A>G | GRCh38 |
| NC_000015.9:g.91292949A>G , CM000677.1:g.91292949A>G | GRCh37 |
| NC_000015.8:g.89093953A>G | NCBI36 |
| NG_007272.1:g.37348A>G , LRG_20:g.37348A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355112.8:c.451A>G MANE Select | ENSP00000347232.3:p.Ile151Val | |
| ENST00000648453.1:c.451A>G | ENSP00000497646.1:p.Ile151Val | |
| ENST00000680772.1:c.451A>G | ENSP00000506117.1:p.Ile151Val | |
| ENST00000681142.1:c.451A>G | ENSP00000506682.1:p.Ile151Val | |
| ENST00000355112.7:c.451A>G | ENSP00000347232.3:p.Ile151Val | |
| ENST00000559282.1:n.625A>G | ||
| ENST00000559724.5:c.451A>G | ENSP00000453359.1:p.Ile151Val | |
| ENST00000560509.5:c.451A>G | ENSP00000454158.1:p.Ile151Val | |
| NM_000057.3:c.451A>G | NP_000048.1:p.Ile151Val | |
| NM_001287246.1:c.451A>G | NP_001274175.1:p.Ile151Val | |
| NM_001287247.1:c.451A>G | NP_001274176.1:p.Ile151Val | |
| NM_001287248.1:c.-841A>G | NP_001274177.1:n.-841A>G | |
| XM_011521882.1:c.451A>G | XP_011520184.1:p.Ile151Val | |
| XM_011521882.3:c.451A>G | XP_011520184.1:p.Ile151Val | |
| NM_000057.4:c.451A>G MANE Select | NP_000048.1:p.Ile151Val | |
| NM_001287246.2:c.451A>G | NP_001274175.1:p.Ile151Val | |
| NM_001287247.2:c.451A>G | NP_001274176.1:p.Ile151Val | |
| NM_001287248.2:c.-841A>G | NP_001274177.1:n.-841A>G |