Linked Data
ClinVar Variation Id:
323316
dbSNP Id:
rs61754348
ExAC:
17:40936108 C / T
gnomAD v2:
17-40936108-C-T
gnomAD v3:
17-42784090-C-T
gnomAD v4:
17-42784090-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42784090C>T , CM000679.2:g.42784090C>T | GRCh38 |
| NC_000017.10:g.40936108C>T , CM000679.1:g.40936108C>T | GRCh37 |
| NC_000017.9:g.38189634C>T | NCBI36 |
| NG_016227.1:g.8460C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000246914.10:c.945C>T MANE Select | ENSP00000246914.4:p.Gly315= | |
| ENST00000246914.9:c.945C>T | ENSP00000246914.4:p.Gly315= | |
| ENST00000591448.5:c.945C>T | ENSP00000467088.1:p.Gly315= | |
| ENST00000592669.1:n.482C>T | ||
| NM_032387.4:c.945C>T | NP_115763.2:p.Gly315= | |
| XM_005257595.3:c.945C>T | XP_005257652.1:p.Gly315= | |
| XM_005257596.2:c.945C>T | XP_005257653.1:p.Gly315= | |
| XM_005257597.3:c.945C>T | XP_005257654.1:p.Gly315= | |
| XM_006722020.2:c.945C>T | XP_006722083.1:p.Gly315= | |
| XM_006722021.1:c.26C>T | XP_006722084.1:p.Ala9Val | |
| XM_006722022.1:c.26C>T | XP_006722085.1:p.Ala9Val | |
| XM_011525132.1:c.945C>T | XP_011523434.1:p.Gly315= | |
| XM_011525133.1:c.945C>T | XP_011523435.1:p.Gly315= | |
| XM_011525134.1:c.945C>T | XP_011523436.1:p.Gly315= | |
| XM_011525135.1:c.945C>T | XP_011523437.1:p.Gly315= | |
| NM_001321299.1:c.26C>T | NP_001308228.1:p.Ala9Val | |
| XM_017024962.1:c.945C>T | XP_016880451.1:p.Gly315= | |
| XM_017024966.1:c.26C>T | XP_016880455.1:p.Ala9Val | |
| NM_032387.5:c.945C>T MANE Select | NP_115763.2:p.Gly315= | |
| NM_001321299.2:c.26C>T | NP_001308228.1:p.Ala9Val |