Linked Data
dbSNP Id:
rs1453851892
gnomAD v2:
15-78894536-T-C
gnomAD v3:
15-78602194-T-C
gnomAD v4:
15-78602194-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.78602194T>C , CM000677.2:g.78602194T>C | GRCh38 |
| NC_000015.9:g.78894536T>C , CM000677.1:g.78894536T>C | GRCh37 |
| NC_000015.8:g.76681591T>C | NCBI36 |
| NG_016143.1:g.24102A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326828.6:c.448A>G MANE Select | ENSP00000315602.5:p.Ile150Val | |
| ENST00000326828.5:c.448A>G | ENSP00000315602.5:p.Ile150Val | |
| ENST00000348639.7:c.448A>G | ENSP00000267951.4:p.Ile150Val | |
| ENST00000558903.1:n.155A>G | ||
| ENST00000559658.5:c.448A>G | ENSP00000452896.1:p.Ile150Val | |
| NM_000743.4:c.448A>G | NP_000734.2:p.Ile150Val | |
| NM_001166694.1:c.448A>G | NP_001160166.1:p.Ile150Val | |
| NR_046313.1:n.949A>G | ||
| XM_006720382.1:c.247A>G | XP_006720445.1:p.Ile83Val | |
| XM_011521173.1:c.367A>G | XP_011519475.1:p.Ile123Val | |
| XM_006720382.3:c.247A>G | XP_006720445.1:p.Ile83Val | |
| NM_000743.5:c.448A>G MANE Select | NP_000734.2:p.Ile150Val | |
| NM_001166694.2:c.448A>G | NP_001160166.1:p.Ile150Val | |
| NR_046313.2:n.650A>G |