Linked Data
ClinVar Variation Id:
46320
dbSNP Id:
rs376900429
ExAC:
5:89949166 T / A
gnomAD v2:
5-89949166-T-A
gnomAD v3:
5-90653349-T-A
gnomAD v4:
5-90653349-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.90653349T>A , CM000667.2:g.90653349T>A | GRCh38 |
| NC_000005.9:g.89949166T>A , CM000667.1:g.89949166T>A | GRCh37 |
| NC_000005.8:g.89984922T>A | NCBI36 |
| NG_007083.1:g.99550T>A | |
| NG_007083.2:g.129006T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000405460.9:c.3775T>A MANE Select | ENSP00000384582.2:p.Ser1259Thr | |
| ENST00000504142.2:n.2541T>A | ||
| ENST00000639676.1:n.1373T>A | ||
| ENST00000640403.1:c.1066T>A | ENSP00000492531.1:p.Ser356Thr | |
| ENST00000405460.6:c.3775T>A | ENSP00000384582.2:p.Ser1259Thr | |
| ENST00000504142.1:c.2540T>A | ||
| NM_032119.3:c.3775T>A | NP_115495.3:p.Ser1259Thr | |
| NR_003149.1:n.3871T>A | ||
| XM_011543675.1:c.3775T>A | XP_011541977.1:p.Ser1259Thr | |
| XM_011543676.1:c.3775T>A | XP_011541978.1:p.Ser1259Thr | |
| XM_011543677.1:c.1078T>A | XP_011541979.1:p.Ser360Thr | |
| XM_011543678.1:c.3775T>A | XP_011541980.1:p.Ser1259Thr | |
| XM_011543679.1:c.3775T>A | XP_011541981.1:p.Ser1259Thr | |
| NM_032119.4:c.3775T>A MANE Select | NP_115495.3:p.Ser1259Thr | |
| XM_017009963.2:c.3775T>A | XP_016865452.1:p.Ser1259Thr | |
| XM_017009964.2:c.3775T>A | XP_016865453.1:p.Ser1259Thr | |
| XM_017009965.1:c.3772T>A | XP_016865454.1:p.Ser1258Thr | |
| XM_017009966.2:c.3775T>A | XP_016865455.1:p.Ser1259Thr | |
| XM_017009967.1:c.3679T>A | XP_016865456.1:p.Ser1227Thr | |
| XM_017009968.2:c.3775T>A | XP_016865457.1:p.Ser1259Thr | |
| XM_017009969.2:c.3775T>A | XP_016865458.1:p.Ser1259Thr | |
| XM_017009970.2:c.3775T>A | XP_016865459.1:p.Ser1259Thr | |
| XM_017009971.2:c.3775T>A | XP_016865460.1:p.Ser1259Thr | |
| XM_017009974.2:c.3775T>A | XP_016865463.1:p.Ser1259Thr | |
| NR_003149.2:n.3874T>A |