Linked Data
ClinVar Variation Id:
308910
dbSNP Id:
rs536885536
ExAC:
12:48369782 A / C
gnomAD v2:
12-48369782-A-C
gnomAD v3:
12-47975999-A-C
gnomAD v4:
12-47975999-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.47975999A>C , CM000674.2:g.47975999A>C | GRCh38 |
| NC_000012.11:g.48369782A>C , CM000674.1:g.48369782A>C | GRCh37 |
| NC_000012.10:g.46656049A>C | NCBI36 |
| NG_008072.1:g.33504T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000337299.7:c.3354T>G | ENSP00000338213.6:p.Pro1118= | |
| ENST00000380518.8:c.3561T>G MANE Select | ENSP00000369889.3:p.Pro1187= | |
| ENST00000337299.6:c.3354T>G | ENSP00000338213.6:p.Pro1118= | |
| ENST00000380518.7:c.3561T>G | ENSP00000369889.3:p.Pro1187= | |
| ENST00000493991.5:n.2647T>G | ||
| ENST00000546974.1:n.414T>G | ||
| NM_001844.4:c.3561T>G | NP_001835.3:p.Pro1187= | |
| NM_033150.2:c.3354T>G | NP_149162.2:p.Pro1118= | |
| XM_006719242.2:c.3705T>G | XP_006719305.2:p.Pro1235= | |
| XM_011537928.1:c.3705T>G | XP_011536230.1:p.Pro1235= | |
| XM_011537929.1:c.3705T>G | XP_011536231.1:p.Pro1235= | |
| XM_011537930.1:c.3705T>G | XP_011536232.1:p.Pro1235= | |
| XM_011537931.1:c.3705T>G | XP_011536233.1:p.Pro1235= | |
| XM_011537932.1:c.3705T>G | XP_011536234.1:p.Pro1235= | |
| XM_011537933.1:c.3705T>G | XP_011536235.1:p.Pro1235= | |
| XM_011537934.1:c.3702T>G | XP_011536236.1:p.Pro1234= | |
| XM_011537935.1:c.2649T>G | XP_011536237.1:p.Pro883= | |
| XM_017018828.1:c.3705T>G | XP_016874317.1:p.Pro1235= | |
| XM_017018829.1:c.3702T>G | XP_016874318.1:p.Pro1234= | |
| XM_017018830.1:c.3495T>G | XP_016874319.1:p.Pro1165= | |
| XM_017018831.2:c.3015T>G | XP_016874320.1:p.Pro1005= | |
| NM_001844.5:c.3561T>G MANE Select | NP_001835.3:p.Pro1187= | |
| NM_033150.3:c.3354T>G | NP_149162.2:p.Pro1118= |