Linked Data
ClinVar Variation Id:
1618526
dbSNP Id:
rs2144088075
MyVariant Identifiers:
chr17:g.59761305G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.61683944G>A , CM000679.2:g.61683944G>A | GRCh38 |
| NC_000017.10:g.59761305G>A , CM000679.1:g.59761305G>A | GRCh37 |
| NC_000017.9:g.57116087G>A | NCBI36 |
| NG_007409.2:g.184616C>T , LRG_300:g.184616C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682073.1:n.1842C>T | ||
| ENST00000682453.1:c.3102C>T | ENSP00000506943.1:p.Pro1034= | |
| ENST00000682477.1:c.*2528C>T | ENSP00000507075.1:n.*2528C>T | |
| ENST00000682589.1:n.8979C>T | ||
| ENST00000682755.1:c.2880C>T | ENSP00000507660.1:p.Pro960= | |
| ENST00000682989.1:c.*193C>T | ENSP00000507786.1:n.*193C>T | |
| ENST00000683039.1:c.3102C>T | ENSP00000508303.1:p.Pro1034= | |
| ENST00000683235.1:c.*517C>T | ENSP00000507646.1:n.*517C>T | |
| ENST00000683535.1:n.1232C>T | ||
| ENST00000684584.1:c.2265C>T | ENSP00000508044.1:p.Pro755= | |
| ENST00000684626.1:n.1348C>T | ||
| ENST00000684769.1:c.1292C>T | ENSP00000507691.1:n.1292C>T | |
| ENST00000259008.7:c.3102C>T MANE Select | ENSP00000259008.2:p.Pro1034= | |
| ENST00000259008.6:c.3102C>T | ENSP00000259008.2:p.Pro1034= | |
| NM_032043.2:c.3102C>T , LRG_300t1:c.3102C>T | NP_114432.2:p.Pro1034= | |
| XM_011525332.1:c.3162C>T | XP_011523634.1:p.Pro1054= | |
| XM_011525333.1:c.3162C>T | XP_011523635.1:p.Pro1054= | |
| XM_011525334.1:c.3162C>T | XP_011523636.1:p.Pro1054= | |
| XM_011525335.1:c.3102C>T | XP_011523637.1:p.Pro1034= | |
| XM_011525336.1:c.3042C>T | XP_011523638.1:p.Pro1014= | |
| XM_011525337.1:c.2961C>T | XP_011523639.1:p.Pro987= | |
| XM_011525338.1:c.2679C>T | XP_011523640.1:p.Pro893= | |
| XM_011525332.3:c.3162C>T | XP_011523634.1:p.Pro1054= | |
| XM_011525333.3:c.3162C>T | XP_011523635.1:p.Pro1054= | |
| XM_011525334.2:c.3162C>T | XP_011523636.1:p.Pro1054= | |
| XM_011525335.3:c.3102C>T | XP_011523637.1:p.Pro1034= | |
| XM_011525336.2:c.3042C>T | XP_011523638.1:p.Pro1014= | |
| XM_011525337.2:c.2961C>T | XP_011523639.1:p.Pro987= | |
| XM_011525338.2:c.2679C>T | XP_011523640.1:p.Pro893= | |
| XM_017025200.1:c.2619C>T | XP_016880689.1:p.Pro873= | |
| XM_017025201.1:c.2619C>T | XP_016880690.1:p.Pro873= | |
| XM_017025202.1:c.1248C>T | XP_016880691.1:p.Pro416= | |
| XM_017025203.1:c.1248C>T | XP_016880692.1:p.Pro416= | |
| NM_032043.3:c.3102C>T MANE Select | NP_114432.2:p.Pro1034= |