Linked Data
ClinVar Variation Id:
183986
dbSNP Id:
rs374335608
ExAC:
17:59763291 A / G
gnomAD v2:
17-59763291-A-G
gnomAD v3:
17-61685930-A-G
gnomAD v4:
17-61685930-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.61685930A>G , CM000679.2:g.61685930A>G | GRCh38 |
| NC_000017.10:g.59763291A>G , CM000679.1:g.59763291A>G | GRCh37 |
| NC_000017.9:g.57118073A>G | NCBI36 |
| NG_007409.2:g.182630T>C , LRG_300:g.182630T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682066.1:c.2941T>C | ENSP00000507191.1:n.2941T>C | |
| ENST00000682073.1:n.1551T>C | ||
| ENST00000682433.1:n.1890T>C | ||
| ENST00000682453.1:c.2811T>C | ENSP00000506943.1:p.Asp937= | |
| ENST00000682477.1:c.*2237T>C | ENSP00000507075.1:n.*2237T>C | |
| ENST00000682589.1:n.8688T>C | ||
| ENST00000682755.1:c.2589T>C | ENSP00000507660.1:p.Asp863= | |
| ENST00000682989.1:c.2610-1790T>C | ENSP00000507786.1:n.2610-1790T>C | |
| ENST00000683039.1:c.2811T>C | ENSP00000508303.1:p.Asp937= | |
| ENST00000683235.1:c.*226T>C | ENSP00000507646.1:n.*226T>C | |
| ENST00000683535.1:n.941T>C | ||
| ENST00000684471.1:n.1224T>C | ||
| ENST00000684584.1:c.2069-1790T>C | ENSP00000508044.1:n.2069-1790T>C | |
| ENST00000684626.1:n.1057T>C | ||
| ENST00000684769.1:c.1001T>C | ENSP00000507691.1:n.1001T>C | |
| ENST00000259008.7:c.2811T>C MANE Select | ENSP00000259008.2:p.Asp937= | |
| ENST00000259008.6:c.2811T>C | ENSP00000259008.2:p.Asp937= | |
| ENST00000577598.5:c.2811T>C | ENSP00000464654.1:p.Asp937= | |
| NM_032043.2:c.2811T>C , LRG_300t1:c.2811T>C | NP_114432.2:p.Asp937= | |
| XM_011525332.1:c.2871T>C | XP_011523634.1:p.Asp957= | |
| XM_011525333.1:c.2871T>C | XP_011523635.1:p.Asp957= | |
| XM_011525334.1:c.2871T>C | XP_011523636.1:p.Asp957= | |
| XM_011525335.1:c.2811T>C | XP_011523637.1:p.Asp937= | |
| XM_011525336.1:c.2751T>C | XP_011523638.1:p.Asp917= | |
| XM_011525337.1:c.2670T>C | XP_011523639.1:p.Asp890= | |
| XM_011525338.1:c.2388T>C | XP_011523640.1:p.Asp796= | |
| XM_011525332.3:c.2871T>C | XP_011523634.1:p.Asp957= | |
| XM_011525333.3:c.2871T>C | XP_011523635.1:p.Asp957= | |
| XM_011525334.2:c.2871T>C | XP_011523636.1:p.Asp957= | |
| XM_011525335.3:c.2811T>C | XP_011523637.1:p.Asp937= | |
| XM_011525336.2:c.2751T>C | XP_011523638.1:p.Asp917= | |
| XM_011525337.2:c.2670T>C | XP_011523639.1:p.Asp890= | |
| XM_011525338.2:c.2388T>C | XP_011523640.1:p.Asp796= | |
| XM_017025200.1:c.2328T>C | XP_016880689.1:p.Asp776= | |
| XM_017025201.1:c.2328T>C | XP_016880690.1:p.Asp776= | |
| XM_017025202.1:c.957T>C | XP_016880691.1:p.Asp319= | |
| XM_017025203.1:c.957T>C | XP_016880692.1:p.Asp319= | |
| NM_032043.3:c.2811T>C MANE Select | NP_114432.2:p.Asp937= |