Linked Data
dbSNP Id:
rs1186451404
gnomAD v2:
17-59760992-G-T
gnomAD v3:
17-61683631-G-T
gnomAD v4:
17-61683631-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.61683631G>T , CM000679.2:g.61683631G>T | GRCh38 |
| NC_000017.10:g.59760992G>T , CM000679.1:g.59760992G>T | GRCh37 |
| NC_000017.9:g.57115774G>T | NCBI36 |
| NG_007409.2:g.184929C>A , LRG_300:g.184929C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682073.1:n.2155C>A | ||
| ENST00000682453.1:c.3415C>A | ENSP00000506943.1:p.Pro1139Thr | |
| ENST00000682477.1:c.*2841C>A | ENSP00000507075.1:n.*2841C>A | |
| ENST00000682589.1:n.9292C>A | ||
| ENST00000682755.1:c.3193C>A | ENSP00000507660.1:p.Pro1065Thr | |
| ENST00000682989.1:c.*506C>A | ENSP00000507786.1:n.*506C>A | |
| ENST00000683039.1:c.3415C>A | ENSP00000508303.1:p.Pro1139Thr | |
| ENST00000683235.1:c.*830C>A | ENSP00000507646.1:n.*830C>A | |
| ENST00000683535.1:n.1545C>A | ||
| ENST00000684584.1:c.2578C>A | ENSP00000508044.1:p.Pro860Thr | |
| ENST00000684626.1:n.1661C>A | ||
| ENST00000684769.1:c.1605C>A | ENSP00000507691.1:n.1605C>A | |
| ENST00000259008.7:c.3415C>A MANE Select | ENSP00000259008.2:p.Pro1139Thr | |
| ENST00000259008.6:c.3415C>A | ENSP00000259008.2:p.Pro1139Thr | |
| NM_032043.2:c.3415C>A , LRG_300t1:c.3415C>A | NP_114432.2:p.Pro1139Thr | |
| XM_011525332.1:c.3475C>A | XP_011523634.1:p.Pro1159Thr | |
| XM_011525333.1:c.3475C>A | XP_011523635.1:p.Pro1159Thr | |
| XM_011525334.1:c.3475C>A | XP_011523636.1:p.Pro1159Thr | |
| XM_011525335.1:c.3415C>A | XP_011523637.1:p.Pro1139Thr | |
| XM_011525336.1:c.3355C>A | XP_011523638.1:p.Pro1119Thr | |
| XM_011525337.1:c.3274C>A | XP_011523639.1:p.Pro1092Thr | |
| XM_011525338.1:c.2992C>A | XP_011523640.1:p.Pro998Thr | |
| XM_011525332.3:c.3475C>A | XP_011523634.1:p.Pro1159Thr | |
| XM_011525333.3:c.3475C>A | XP_011523635.1:p.Pro1159Thr | |
| XM_011525334.2:c.3475C>A | XP_011523636.1:p.Pro1159Thr | |
| XM_011525335.3:c.3415C>A | XP_011523637.1:p.Pro1139Thr | |
| XM_011525336.2:c.3355C>A | XP_011523638.1:p.Pro1119Thr | |
| XM_011525337.2:c.3274C>A | XP_011523639.1:p.Pro1092Thr | |
| XM_011525338.2:c.2992C>A | XP_011523640.1:p.Pro998Thr | |
| XM_017025200.1:c.2932C>A | XP_016880689.1:p.Pro978Thr | |
| XM_017025201.1:c.2932C>A | XP_016880690.1:p.Pro978Thr | |
| XM_017025202.1:c.1561C>A | XP_016880691.1:p.Pro521Thr | |
| XM_017025203.1:c.1561C>A | XP_016880692.1:p.Pro521Thr | |
| NM_032043.3:c.3415C>A MANE Select | NP_114432.2:p.Pro1139Thr |