Linked Data
ClinVar Variation Id:
323845
dbSNP Id:
rs11657819
gnomAD v2:
17-45017837-G-A
gnomAD v3:
17-46940471-G-A
gnomAD v4:
17-46940471-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.46940471G>A , CM000679.2:g.46940471G>A | GRCh38 |
| NC_000017.10:g.45017837G>A , CM000679.1:g.45017837G>A | GRCh37 |
| NC_000017.9:g.42372836G>A | NCBI36 |
| NG_031806.1:g.22352G>A | |
| NG_031806.2:g.22352G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225567.9:c.584-84G>A (GOSR2) | ENSP00000225567.4:n.584-84G>A | |
| ENST00000573224.2:c.583+1767G>A (GOSR2) | ENSP00000461784.2:n.583+1767G>A | |
| ENST00000638189.1:c.583+1767G>A (GOSR2) | ENSP00000491785.1:n.583+1767G>A | |
| ENST00000638216.1:c.*1711G>A (GOSR2) | ENSP00000491961.1:n.*1711G>A | |
| ENST00000638219.1:c.583+1767G>A (GOSR2) | ENSP00000491399.1:n.583+1767G>A | |
| ENST00000638374.1:c.*1711G>A (GOSR2) | ENSP00000492139.1:n.*1711G>A | |
| ENST00000638468.1:c.336+1767G>A (GOSR2) | ||
| ENST00000638579.1:c.583+1767G>A (GOSR2) | ENSP00000491266.1:n.583+1767G>A | |
| ENST00000638634.1:c.*1711G>A (GOSR2) | ENSP00000491946.1:n.*1711G>A | |
| ENST00000638697.1:c.452G>A (GOSR2) | ENSP00000492360.1:p.Arg151Gln | |
| ENST00000638838.1:c.*1711G>A (GOSR2) | ENSP00000492524.1:n.*1711G>A | |
| ENST00000638892.1:c.*1711G>A (GOSR2) | ENSP00000492607.1:n.*1711G>A | |
| ENST00000639066.1:n.475+1767G>A (GOSR2) | ||
| ENST00000639199.1:c.442+1767G>A (GOSR2) | ENSP00000491396.1:n.442+1767G>A | |
| ENST00000639365.1:c.583+1767G>A (GOSR2) | ENSP00000491253.1:n.583+1767G>A | |
| ENST00000639388.1:c.529+1767G>A (GOSR2) | ENSP00000492544.1:n.529+1767G>A | |
| ENST00000639713.1:c.454+1767G>A (GOSR2) | ENSP00000491100.1:n.454+1767G>A | |
| ENST00000639822.1:n.475+1767G>A | ||
| ENST00000639985.1:c.442+1767G>A (GOSR2) | ENSP00000492396.1:n.442+1767G>A | |
| ENST00000640051.2:c.*1711G>A (GOSR2) MANE Select | ENSP00000492751.1:n.*1711G>A | |
| ENST00000640068.1:c.*1711G>A (GOSR2) | ENSP00000491682.1:n.*1711G>A | |
| ENST00000640138.1:c.*1711G>A (GOSR2) | ENSP00000492565.1:n.*1711G>A | |
| ENST00000640358.1:c.583+1767G>A (GOSR2) | ENSP00000491135.1:n.583+1767G>A | |
| ENST00000640443.1:c.*1711G>A (GOSR2) | ENSP00000492548.1:n.*1711G>A | |
| ENST00000640495.1:c.*1711G>A (GOSR2) | ENSP00000491859.1:n.*1711G>A | |
| ENST00000640608.1:c.*1711G>A (GOSR2) | ENSP00000491979.1:n.*1711G>A | |
| ENST00000640711.1:c.*49-84G>A (GOSR2) | ENSP00000491361.1:n.*49-84G>A | |
| ENST00000640723.1:c.522+1767G>A (GOSR2) | ||
| ENST00000640792.1:c.583+1767G>A (GOSR2) | ENSP00000492736.1:n.583+1767G>A | |
| ENST00000640866.1:c.100+1767G>A (GOSR2) | ENSP00000491863.1:n.100+1767G>A | |
| ENST00000225567.8:c.584-84G>A (GOSR2) | ENSP00000225567.4:n.584-84G>A | |
| ENST00000571841.1:c.583+1767G>A | ENSP00000461460.1:n.583+1767G>A | |
| ENST00000572403.5:c.388+1767G>A (GOSR2) | ENSP00000460760.1:n.388+1767G>A | |
| ENST00000573224.1:c.106+1767G>A (GOSR2) | ENSP00000461784.1:n.106+1767G>A | |
| NM_004287.3:c.*1711G>A (GOSR2) | NP_004278.2:n.*1711G>A | |
| NM_054022.2:c.584-84G>A (GOSR2) | NP_473363.1:n.584-84G>A | |
| XM_005257843.2:c.583+1767G>A (GOSR2) | XP_005257900.1:n.583+1767G>A | |
| XM_005257844.2:c.*1711G>A (GOSR2) | XP_005257901.1:n.*1711G>A | |
| XM_005257845.2:c.*1711G>A (GOSR2) | XP_005257902.1:n.*1711G>A | |
| XM_006722190.2:c.583+1767G>A (GOSR2) | XP_006722253.1:n.583+1767G>A | |
| XM_011525497.1:c.583+1767G>A (GOSR2) | XP_011523799.1:n.583+1767G>A | |
| XM_011525498.1:c.529+1767G>A (GOSR2) | XP_011523800.1:n.529+1767G>A | |
| XM_011525499.1:c.442+1767G>A (GOSR2) | XP_011523801.1:n.442+1767G>A | |
| XM_011525500.1:c.583+1767G>A (GOSR2) | XP_011523802.1:n.583+1767G>A | |
| XM_011525501.1:c.583+1767G>A (GOSR2) | XP_011523803.1:n.583+1767G>A | |
| XM_011525502.1:c.583+1767G>A (GOSR2) | XP_011523804.1:n.583+1767G>A | |
| XM_011525503.1:c.442+1767G>A (GOSR2) | XP_011523805.1:n.442+1767G>A | |
| XR_934613.1:n.662+1767G>A (GOSR2) | ||
| XR_934614.1:n.662+1767G>A (GOSR2) | ||
| XR_934615.1:n.662+1767G>A (GOSR2) | ||
| XR_934616.1:n.662+1767G>A (GOSR2) | ||
| XR_934617.1:n.662+1767G>A (GOSR2) | ||
| XR_934618.1:n.662+1767G>A (GOSR2) | ||
| XR_934619.1:n.662+1767G>A (GOSR2) | ||
| XR_934620.1:n.662+1767G>A (GOSR2) | ||
| XR_934621.1:n.875+1767G>A (GOSR2) | ||
| NM_001321133.1:c.583+1767G>A (GOSR2) | NP_001308062.1:n.583+1767G>A | |
| NM_001321134.1:c.*1711G>A (GOSR2) | NP_001308063.1:n.*1711G>A | |
| NM_001330252.1:c.*1711G>A (GOSR2) | NP_001317181.1:n.*1711G>A | |
| NM_001353114.1:c.*1711G>A (GOSR2) | NP_001340043.1:n.*1711G>A | |
| NM_001353115.1:c.*1711G>A (GOSR2) | NP_001340044.1:n.*1711G>A | |
| NM_001353116.1:c.440-84G>A (GOSR2) | NP_001340045.1:n.440-84G>A | |
| NM_001363851.1:c.*1711G>A (GOSR2) | NP_001350780.1:n.*1711G>A | |
| NM_004287.4:c.*1711G>A (GOSR2) | NP_004278.2:n.*1711G>A | |
| NM_054022.3:c.584-84G>A (GOSR2) | NP_473363.1:n.584-84G>A | |
| NR_148349.1:n.659+1767G>A (GOSR2) | ||
| NR_148350.1:n.518+1767G>A (GOSR2) | ||
| NR_148351.1:n.518+1767G>A (GOSR2) | ||
| XM_006722190.4:c.583+1767G>A (GOSR2) | XP_006722253.1:n.583+1767G>A | |
| XM_011525501.3:c.583+1767G>A (GOSR2) | XP_011523803.1:n.583+1767G>A | |
| XM_011525502.3:c.583+1767G>A (GOSR2) | XP_011523804.1:n.583+1767G>A | |
| XM_017025378.1:c.580+1767G>A (GOSR2) | XP_016880867.1:n.580+1767G>A | |
| XM_017025379.1:c.529+1767G>A (GOSR2) | XP_016880868.1:n.529+1767G>A | |
| XM_017025380.1:c.529+1767G>A (GOSR2) | XP_016880869.1:n.529+1767G>A | |
| XM_017025381.1:c.526+1767G>A (GOSR2) | XP_016880870.1:n.526+1767G>A | |
| XM_017025382.1:c.526+1767G>A (GOSR2) | XP_016880871.1:n.526+1767G>A | |
| XM_017025383.2:c.583+1767G>A (GOSR2) | XP_016880872.1:n.583+1767G>A | |
| XM_017025386.1:c.442+1767G>A (GOSR2) | XP_016880875.1:n.442+1767G>A | |
| XM_017025387.1:c.439+1767G>A (GOSR2) | XP_016880876.1:n.439+1767G>A | |
| XM_017025389.1:c.*1711G>A (GOSR2) | XP_016880878.1:n.*1711G>A | |
| XM_017025392.1:c.442+1767G>A (GOSR2) | XP_016880881.1:n.442+1767G>A | |
| XM_017025394.1:c.388+1767G>A (GOSR2) | XP_016880883.1:n.388+1767G>A | |
| XM_017025395.1:c.*1711G>A (GOSR2) | XP_016880884.1:n.*1711G>A | |
| XM_024450773.1:c.4810-108585G>A (LRRC37A2) | XP_024306541.1:n.4810-108585G>A | |
| XR_001752696.2:n.643+1767G>A (GOSR2) | ||
| XR_002958091.1:n.643+1767G>A (GOSR2) | ||
| XR_002958092.1:n.643+1767G>A (GOSR2) | ||
| XR_002958093.1:n.1018+1767G>A (GOSR2) | ||
| XR_934616.3:n.643+1767G>A (GOSR2) | ||
| XR_934619.3:n.643+1767G>A (GOSR2) | ||
| NM_001321133.2:c.583+1767G>A (GOSR2) | NP_001308062.1:n.583+1767G>A | |
| NM_001353116.2:c.440-84G>A (GOSR2) | NP_001340045.1:n.440-84G>A | |
| NM_004287.5:c.*1711G>A (GOSR2) MANE Select | NP_004278.2:n.*1711G>A | |
| NM_054022.4:c.584-84G>A (GOSR2) | NP_473363.1:n.584-84G>A | |
| NR_148349.2:n.616+1767G>A (GOSR2) | ||
| NR_148350.2:n.475+1767G>A (GOSR2) | ||
| NR_148351.2:n.475+1767G>A (GOSR2) | ||
| NM_001321134.2:c.*1711G>A (GOSR2) | NP_001308063.1:n.*1711G>A | |
| NM_001330252.2:c.*1711G>A (GOSR2) | NP_001317181.1:n.*1711G>A | |
| NM_001353114.2:c.*1711G>A (GOSR2) | NP_001340043.1:n.*1711G>A | |
| NM_001353115.2:c.*1711G>A (GOSR2) | NP_001340044.1:n.*1711G>A | |
| NM_001363851.2:c.*1711G>A (GOSR2) | NP_001350780.1:n.*1711G>A |