Linked Data
ClinVar Variation Id:
448973
dbSNP Id:
rs767723985
ExAC:
7:150649728 C / A
gnomAD v2:
7-150649728-C-A
gnomAD v3:
7-150952640-C-A
gnomAD v4:
7-150952640-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150952640C>A , CM000669.2:g.150952640C>A | GRCh38 |
| NC_000007.13:g.150649728C>A , CM000669.1:g.150649728C>A | GRCh37 |
| NC_000007.12:g.150280661C>A | NCBI36 |
| NG_008916.1:g.30287G>T , LRG_288:g.30287G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461280.2:n.640G>T | ||
| ENST00000684116.1:n.235G>T | ||
| ENST00000684241.1:n.2175G>T | ||
| ENST00000262186.10:c.1342G>T MANE Select | ENSP00000262186.5:p.Ala448Ser | |
| ENST00000330883.9:c.322G>T | ENSP00000328531.4:p.Ala108Ser | |
| ENST00000262186.9:c.1342G>T | ENSP00000262186.5:p.Ala448Ser | |
| ENST00000330883.8:c.322G>T | ENSP00000328531.4:p.Ala108Ser | |
| ENST00000430723.4:c.994G>T | ENSP00000387657.4:p.Ala332Ser | |
| ENST00000461280.1:n.629G>T | ||
| ENST00000473610.5:n.647G>T | ||
| ENST00000532957.5:n.1565G>T | ||
| NM_000238.3:c.1342G>T , LRG_288t1:c.1342G>T | NP_000229.1:p.Ala448Ser | |
| NM_001204798.1:c.322G>T | NP_001191727.1:p.Ala108Ser | |
| NM_172056.2:c.1342G>T , LRG_288t2:c.1342G>T | NP_742053.1:p.Ala448Ser | |
| NM_172057.2:c.322G>T , LRG_288t3:c.322G>T | NP_742054.1:p.Ala108Ser | |
| XM_011516185.1:c.1042G>T | XP_011514487.1:p.Ala348Ser | |
| XM_011516186.1:c.1342G>T | XP_011514488.1:p.Ala448Ser | |
| XM_011516185.2:c.1042G>T | XP_011514487.1:p.Ala348Ser | |
| XM_011516186.3:c.1342G>T | XP_011514488.1:p.Ala448Ser | |
| XM_017012195.1:c.1192G>T | XP_016867684.1:p.Ala398Ser | |
| XM_017012196.1:c.1165G>T | XP_016867685.1:p.Ala389Ser | |
| NM_000238.4:c.1342G>T MANE Select | NP_000229.1:p.Ala448Ser | |
| NM_001204798.2:c.322G>T | NP_001191727.1:p.Ala108Ser | |
| NM_172057.3:c.322G>T | NP_742054.1:p.Ala108Ser |