Linked Data
ClinVar Variation Id:
45869
dbSNP Id:
rs200324241
ExAC:
10:73406371 C / A
gnomAD v2:
10-73406371-C-A
gnomAD v3:
10-71646614-C-A
gnomAD v4:
10-71646614-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.71646614C>A , CM000672.2:g.71646614C>A | GRCh38 |
| NC_000010.10:g.73406371C>A , CM000672.1:g.73406371C>A | GRCh37 |
| NC_000010.9:g.73076377C>A | NCBI36 |
| NG_008835.1:g.254668C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000224721.12:c.1446C>A MANE Select | ENSP00000224721.9:p.Val482= | |
| ENST00000398809.9:c.1446C>A | ENSP00000381789.5:p.Val482= | |
| ENST00000442677.4:c.1446C>A | ENSP00000388894.3:p.Val482= | |
| ENST00000466757.8:c.877C>A | ||
| ENST00000643732.1:n.1282C>A | ||
| ENST00000646131.1:c.1110C>A | ENSP00000495098.1:p.Val370= | |
| ENST00000224721.10:c.1461C>A | ENSP00000224721.8:p.Val487= | |
| ENST00000299366.11:c.1446C>A | ENSP00000299366.8:p.Val482= | |
| ENST00000398809.8:c.1446C>A | ENSP00000381789.5:p.Val482= | |
| ENST00000398842.7:c.1191C>A | ENSP00000381822.4:p.Val397= | |
| ENST00000442677.3:c.221C>A | ||
| ENST00000461841.7:c.1446C>A | ENSP00000473454.2:p.Val482= | |
| ENST00000466757.7:c.877C>A | ||
| ENST00000470494.5:c.415C>A | ||
| ENST00000616684.4:c.1446C>A | ENSP00000482036.2:p.Val482= | |
| ENST00000622827.4:c.1446C>A | ENSP00000483211.1:p.Val482= | |
| NM_001171930.1:c.1446C>A | NP_001165401.1:p.Val482= | |
| NM_001171931.1:c.1446C>A | NP_001165402.1:p.Val482= | |
| NM_022124.5:c.1446C>A | NP_071407.4:p.Val482= | |
| NM_052836.3:c.1446C>A | NP_443068.1:p.Val482= | |
| XM_006717940.2:c.1641C>A | XP_006718003.1:p.Val547= | |
| XM_006717942.2:c.1575C>A | XP_006718005.1:p.Val525= | |
| XM_011540039.1:c.1641C>A | XP_011538341.1:p.Val547= | |
| XM_011540040.1:c.1635C>A | XP_011538342.1:p.Val545= | |
| XM_011540041.1:c.1581C>A | XP_011538343.1:p.Val527= | |
| XM_011540042.1:c.1641C>A | XP_011538344.1:p.Val547= | |
| XM_011540043.1:c.1641C>A | XP_011538345.1:p.Val547= | |
| XM_011540044.1:c.1506C>A | XP_011538346.1:p.Val502= | |
| XM_011540045.1:c.1641C>A | XP_011538347.1:p.Val547= | |
| XM_011540046.1:c.1101C>A | XP_011538348.1:p.Val367= | |
| XM_011540047.1:c.459C>A | XP_011538349.1:p.Val153= | |
| XM_011540048.1:c.1641C>A | XP_011538350.1:p.Val547= | |
| XM_011540049.1:c.1641C>A | XP_011538351.1:p.Val547= | |
| XM_011540050.1:c.1641C>A | XP_011538352.1:p.Val547= | |
| XM_011540051.1:c.1641C>A | XP_011538353.1:p.Val547= | |
| XM_011540053.1:c.1641C>A | XP_011538355.1:p.Val547= | |
| XM_011540054.1:c.1581C>A | XP_011538356.1:p.Val527= | |
| XR_945796.1:n.1884C>A | ||
| NM_001171930.2:c.1446C>A | NP_001165401.1:p.Val482= | |
| NM_001171931.2:c.1446C>A | NP_001165402.1:p.Val482= | |
| NM_022124.6:c.1446C>A MANE Select | NP_071407.4:p.Val482= | |
| NM_052836.4:c.1446C>A | NP_443068.1:p.Val482= |