Linked Data
ClinVar Variation Id:
733489
dbSNP Id:
rs150927045
ExAC:
17:19575224 C / T
gnomAD v2:
17-19575224-C-T
gnomAD v3:
17-19671911-C-T
gnomAD v4:
17-19671911-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.19671911C>T , CM000679.2:g.19671911C>T | GRCh38 |
| NC_000017.10:g.19575224C>T , CM000679.1:g.19575224C>T | GRCh37 |
| NC_000017.9:g.19515816C>T | NCBI36 |
| NG_007095.2:g.28161C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000176643.11:c.1398C>T MANE Select | ENSP00000176643.6:p.Leu466= | |
| ENST00000395575.7:c.1071C>T | ENSP00000378942.3:p.Leu357= | |
| ENST00000472059.6:c.*956C>T | ENSP00000458397.1:n.*956C>T | |
| ENST00000571163.2:c.227-3585C>T | ENSP00000459977.2:n.227-3585C>T | |
| ENST00000573947.2:c.198C>T | ENSP00000462933.2:p.Leu66= | |
| ENST00000574078.3:n.727C>T | ||
| ENST00000581518.6:c.1398C>T | ENSP00000461916.2:p.Leu466= | |
| ENST00000582991.6:c.*116C>T | ENSP00000464153.1:n.*116C>T | |
| ENST00000671878.1:c.1398C>T | ENSP00000500516.1:p.Leu466= | |
| ENST00000672059.1:n.1749C>T | ||
| ENST00000672357.1:c.1398C>T | ENSP00000500092.1:p.Leu466= | |
| ENST00000672465.1:c.1398C>T | ENSP00000500517.1:p.Leu466= | |
| ENST00000672487.1:c.*578C>T | ENSP00000500740.1:n.*578C>T | |
| ENST00000672564.1:n.3067C>T | ||
| ENST00000672567.1:c.1098+6864C>T | ||
| ENST00000672591.1:c.458C>T | ||
| ENST00000672608.1:n.2387C>T | ||
| ENST00000672709.1:c.1252C>T | ||
| ENST00000673064.1:n.1898C>T | ||
| ENST00000673136.1:c.1208-3585C>T | ENSP00000500380.1:n.1208-3585C>T | |
| ENST00000673472.1:n.1734C>T | ||
| ENST00000673516.1:n.1858C>T | ||
| ENST00000176643.10:c.1398C>T | ENSP00000176643.6:p.Leu466= | |
| ENST00000339618.8:c.1398C>T | ENSP00000345774.4:p.Leu466= | |
| ENST00000395575.6:c.1398C>T | ENSP00000378942.2:p.Leu466= | |
| ENST00000472059.5:c.*956C>T | ENSP00000458397.1:n.*956C>T | |
| ENST00000476965.5:n.1148C>T | ||
| ENST00000571163.1:c.227-3647C>T | ENSP00000459977.1:n.227-3647C>T | |
| ENST00000573565.1:c.113C>T | ||
| ENST00000573947.1:c.305C>T | ENSP00000462933.1:n.305C>T | |
| ENST00000575384.2:c.144C>T | ENSP00000461235.2:p.Leu48= | |
| ENST00000579855.5:c.1398C>T | ENSP00000463637.1:p.Leu466= | |
| ENST00000581518.5:c.1398C>T | ENSP00000461916.1:p.Leu466= | |
| ENST00000582991.5:c.*116C>T | ENSP00000464153.1:n.*116C>T | |
| ENST00000630662.2:c.227-3647C>T | ENSP00000487353.1:n.227-3647C>T | |
| ENST00000631291.2:c.*116C>T | ENSP00000486085.1:n.*116C>T | |
| NM_000382.2:c.1398C>T | NP_000373.1:p.Leu466= | |
| NM_001031806.1:c.1398C>T | NP_001026976.1:p.Leu466= | |
| XM_011523732.1:c.1398C>T | XP_011522034.1:p.Leu466= | |
| XM_011523733.1:c.1398C>T | XP_011522035.1:p.Leu466= | |
| XM_011523733.2:c.1398C>T | XP_011522035.1:p.Leu466= | |
| XM_017024355.1:c.1208-3647C>T | XP_016879844.1:n.1208-3647C>T | |
| XM_017024356.2:c.1398C>T | XP_016879845.1:p.Leu466= | |
| XM_017024357.1:c.1398C>T | XP_016879846.1:p.Leu466= | |
| XM_017024358.2:c.1208-3647C>T | XP_016879847.1:n.1208-3647C>T | |
| XM_024450651.1:c.819C>T | XP_024306419.1:p.Leu273= | |
| XM_024450652.1:c.819C>T | XP_024306420.1:p.Leu273= | |
| NM_000382.3:c.1398C>T MANE Select | NP_000373.1:p.Leu466= | |
| NM_001031806.2:c.1398C>T | NP_001026976.1:p.Leu466= | |
| NM_001369136.1:c.1398C>T | NP_001356065.1:p.Leu466= | |
| NM_001369137.1:c.1398C>T | NP_001356066.1:p.Leu466= | |
| NM_001369138.1:c.1398C>T | NP_001356067.1:p.Leu466= | |
| NM_001369139.1:c.1398C>T | NP_001356068.1:p.Leu466= | |
| NM_001369146.1:c.1208-3647C>T | NP_001356075.1:n.1208-3647C>T | |
| NM_001369148.1:c.819C>T | NP_001356077.1:p.Leu273= | |
| NM_001369137.2:c.1398C>T | NP_001356066.1:p.Leu466= | |
| NM_001369138.2:c.1398C>T | NP_001356067.1:p.Leu466= | |
| NM_001369146.2:c.1208-3647C>T | NP_001356075.1:n.1208-3647C>T | |
| NM_001369148.2:c.819C>T | NP_001356077.1:p.Leu273= |