Linked Data
ClinVar Variation Id:
185173
ClinVar RCV Id:
RCV000164542
RCV000472623
RCV000432753
RCV000989973
RCV001124767
RCV001704197
RCV004535101
dbSNP Id:
rs764848326
ExAC:
17:59760840 A / G
gnomAD v2:
17-59760840-A-G
gnomAD v3:
17-61683479-A-G
gnomAD v4:
17-61683479-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.61683479A>G , CM000679.2:g.61683479A>G | GRCh38 |
| NC_000017.10:g.59760840A>G , CM000679.1:g.59760840A>G | GRCh37 |
| NC_000017.9:g.57115622A>G | NCBI36 |
| NG_007409.2:g.185081T>C , LRG_300:g.185081T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682073.1:n.2307T>C | ||
| ENST00000682453.1:c.3567T>C | ENSP00000506943.1:p.Asp1189= | |
| ENST00000682477.1:c.*2993T>C | ENSP00000507075.1:n.*2993T>C | |
| ENST00000682589.1:n.9444T>C | ||
| ENST00000682755.1:c.3345T>C | ENSP00000507660.1:p.Asp1115= | |
| ENST00000682989.1:c.*658T>C | ENSP00000507786.1:n.*658T>C | |
| ENST00000683039.1:c.3567T>C | ENSP00000508303.1:p.Asp1189= | |
| ENST00000683235.1:c.*982T>C | ENSP00000507646.1:n.*982T>C | |
| ENST00000683535.1:n.1697T>C | ||
| ENST00000684584.1:c.2730T>C | ENSP00000508044.1:p.Asp910= | |
| ENST00000684626.1:n.1813T>C | ||
| ENST00000684769.1:c.1757T>C | ENSP00000507691.1:n.1757T>C | |
| ENST00000259008.7:c.3567T>C MANE Select | ENSP00000259008.2:p.Asp1189= | |
| ENST00000259008.6:c.3567T>C | ENSP00000259008.2:p.Asp1189= | |
| NM_032043.2:c.3567T>C , LRG_300t1:c.3567T>C | NP_114432.2:p.Asp1189= | |
| XM_011525332.1:c.3627T>C | XP_011523634.1:p.Asp1209= | |
| XM_011525333.1:c.3627T>C | XP_011523635.1:p.Asp1209= | |
| XM_011525334.1:c.3627T>C | XP_011523636.1:p.Asp1209= | |
| XM_011525335.1:c.3567T>C | XP_011523637.1:p.Asp1189= | |
| XM_011525336.1:c.3507T>C | XP_011523638.1:p.Asp1169= | |
| XM_011525337.1:c.3426T>C | XP_011523639.1:p.Asp1142= | |
| XM_011525338.1:c.3144T>C | XP_011523640.1:p.Asp1048= | |
| XM_011525332.3:c.3627T>C | XP_011523634.1:p.Asp1209= | |
| XM_011525333.3:c.3627T>C | XP_011523635.1:p.Asp1209= | |
| XM_011525334.2:c.3627T>C | XP_011523636.1:p.Asp1209= | |
| XM_011525335.3:c.3567T>C | XP_011523637.1:p.Asp1189= | |
| XM_011525336.2:c.3507T>C | XP_011523638.1:p.Asp1169= | |
| XM_011525337.2:c.3426T>C | XP_011523639.1:p.Asp1142= | |
| XM_011525338.2:c.3144T>C | XP_011523640.1:p.Asp1048= | |
| XM_017025200.1:c.3084T>C | XP_016880689.1:p.Asp1028= | |
| XM_017025201.1:c.3084T>C | XP_016880690.1:p.Asp1028= | |
| XM_017025202.1:c.1713T>C | XP_016880691.1:p.Asp571= | |
| XM_017025203.1:c.1713T>C | XP_016880692.1:p.Asp571= | |
| NM_032043.3:c.3567T>C MANE Select | NP_114432.2:p.Asp1189= |