Linked Data
ClinVar Variation Id:
365298
dbSNP Id:
rs112845474
gnomAD v2:
9-134399128-T-G
gnomAD v3:
9-131523741-T-G
gnomAD v4:
9-131523741-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.131523741T>G , CM000671.2:g.131523741T>G | GRCh38 |
| NC_000009.11:g.134399128T>G , CM000671.1:g.134399128T>G | GRCh37 |
| NC_000009.10:g.133388949T>G | NCBI36 |
| NG_008896.1:g.25840T>G | |
| NG_008896.2:g.25840T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341012.13:c.*635T>G | ENSP00000343034.7:n.*635T>G | |
| ENST00000404875.7:n.3353T>G | ||
| ENST00000677295.2:c.*3157T>G | ENSP00000504346.2:n.*3157T>G | |
| ENST00000678264.2:c.*2996T>G | ENSP00000503157.2:n.*2996T>G | |
| ENST00000682639.1:c.518T>G | ||
| ENST00000682813.1:n.3210T>G | ||
| ENST00000683231.1:c.663T>G | ||
| ENST00000683900.1:n.4713T>G | ||
| ENST00000684062.1:n.3479T>G | ||
| ENST00000684399.1:c.628T>G | ||
| ENST00000684579.1:n.4659T>G | ||
| ENST00000341012.12:c.*635T>G | ENSP00000343034.7:n.*635T>G | |
| ENST00000372228.9:c.*635T>G | ENSP00000361302.3:n.*635T>G | |
| ENST00000402686.8:c.*635T>G MANE Select | ENSP00000385797.4:n.*635T>G | |
| ENST00000676640.1:c.*635T>G | ENSP00000503281.1:n.*635T>G | |
| ENST00000676835.1:c.*2028T>G | ENSP00000502911.1:n.*2028T>G | |
| ENST00000677444.1:c.2758T>G | ||
| ENST00000678546.1:c.*2758T>G | ENSP00000503062.1:n.*2758T>G | |
| ENST00000678833.1:c.*2565T>G | ENSP00000503893.1:n.*2565T>G | |
| ENST00000679023.1:c.*459T>G | ENSP00000503718.1:n.*459T>G | |
| ENST00000679111.1:c.*1569T>G | ENSP00000504257.1:n.*1569T>G | |
| ENST00000341012.11:c.*635T>G | ENSP00000343034.7:n.*635T>G | |
| ENST00000372220.4:c.1676T>G | ENSP00000361294.4:n.1676T>G | |
| ENST00000372228.7:c.*635T>G | ENSP00000361302.3:n.*635T>G | |
| ENST00000402686.7:c.*635T>G | ENSP00000385797.3:n.*635T>G | |
| ENST00000404875.6:c.*635T>G | ENSP00000384531.2:n.*635T>G | |
| ENST00000423007.5:c.*635T>G | ENSP00000404119.1:n.*635T>G | |
| ENST00000485278.5:n.3363T>G | ||
| NM_001077365.1:c.*635T>G | NP_001070833.1:n.*635T>G | |
| NM_001077366.1:c.*635T>G | NP_001070834.1:n.*635T>G | |
| NM_001136113.1:c.*635T>G | NP_001129585.1:n.*635T>G | |
| NM_001136114.1:c.*635T>G | NP_001129586.1:n.*635T>G | |
| NM_007171.3:c.*635T>G | NP_009102.3:n.*635T>G | |
| XM_005272156.1:c.*635T>G | XP_005272213.1:n.*635T>G | |
| XM_005272158.1:c.*635T>G | XP_005272215.1:n.*635T>G | |
| XM_005272159.1:c.*635T>G | XP_005272216.1:n.*635T>G | |
| XM_005272162.1:c.*635T>G | XP_005272219.1:n.*635T>G | |
| XM_006716932.1:c.*635T>G | XP_006716995.1:n.*635T>G | |
| XM_011518140.1:c.*635T>G | XP_011516442.1:n.*635T>G | |
| XM_011518141.1:c.*635T>G | XP_011516443.1:n.*635T>G | |
| XM_011518142.1:c.*635T>G | XP_011516444.1:n.*635T>G | |
| XM_011518143.1:c.*635T>G | XP_011516445.1:n.*635T>G | |
| XM_011518145.1:c.*635T>G | XP_011516447.1:n.*635T>G | |
| XM_011518147.1:c.*635T>G | XP_011516449.1:n.*635T>G | |
| XR_929703.1:n.2879T>G | ||
| NM_001353193.1:c.*635T>G | NP_001340122.1:n.*635T>G | |
| NM_001353194.1:c.*635T>G | NP_001340123.1:n.*635T>G | |
| NM_001353195.1:c.*635T>G | NP_001340124.1:n.*635T>G | |
| NM_001353196.1:c.*635T>G | NP_001340125.1:n.*635T>G | |
| NM_001353197.1:c.*635T>G | NP_001340126.1:n.*635T>G | |
| NM_001353198.1:c.*635T>G | NP_001340127.1:n.*635T>G | |
| NM_001353199.1:c.*635T>G | NP_001340128.1:n.*635T>G | |
| NM_001353200.1:c.*635T>G | NP_001340129.1:n.*635T>G | |
| NR_148391.1:n.2687T>G | ||
| NR_148392.1:n.2905T>G | ||
| NR_148393.1:n.3002T>G | ||
| NR_148394.1:n.2756T>G | ||
| NR_148395.1:n.3154T>G | ||
| NR_148396.1:n.2788T>G | ||
| NR_148397.1:n.2913T>G | ||
| NR_148398.1:n.2868T>G | ||
| NR_148399.1:n.3218T>G | ||
| NR_148400.1:n.2993T>G | ||
| XM_005272162.3:c.*635T>G | XP_005272219.1:n.*635T>G | |
| XM_006716932.2:c.*635T>G | XP_006716995.1:n.*635T>G | |
| XM_011518140.2:c.*635T>G | XP_011516442.1:n.*635T>G | |
| XM_011518141.2:c.*635T>G | XP_011516443.1:n.*635T>G | |
| XM_011518142.2:c.*635T>G | XP_011516444.1:n.*635T>G | |
| XM_011518143.2:c.*635T>G | XP_011516445.1:n.*635T>G | |
| XM_011518145.2:c.*635T>G | XP_011516447.1:n.*635T>G | |
| XM_017014205.2:c.*635T>G | XP_016869694.1:n.*635T>G | |
| XM_024447380.1:c.*635T>G | XP_024303148.1:n.*635T>G | |
| XM_024447381.1:c.*635T>G | XP_024303149.1:n.*635T>G | |
| XM_024447382.1:c.*635T>G | XP_024303150.1:n.*635T>G | |
| XR_001746160.2:n.2807T>G | ||
| XR_001746162.2:n.3188T>G | ||
| XR_001746164.1:n.2905T>G | ||
| XR_001746166.2:n.3024T>G | ||
| NM_001077365.2:c.*635T>G MANE Select | NP_001070833.1:n.*635T>G | |
| NM_001077366.2:c.*635T>G | NP_001070834.1:n.*635T>G | |
| NM_001136113.2:c.*635T>G | NP_001129585.1:n.*635T>G | |
| NM_001136114.2:c.*635T>G | NP_001129586.1:n.*635T>G | |
| NM_001353193.2:c.*635T>G | NP_001340122.2:n.*635T>G | |
| NM_001353194.2:c.*635T>G | NP_001340123.1:n.*635T>G | |
| NM_001353195.2:c.*635T>G | NP_001340124.1:n.*635T>G | |
| NM_001353196.2:c.*635T>G | NP_001340125.1:n.*635T>G | |
| NM_001353197.2:c.*635T>G | NP_001340126.2:n.*635T>G | |
| NM_001353198.2:c.*635T>G | NP_001340127.2:n.*635T>G | |
| NM_001353199.2:c.*635T>G | NP_001340128.2:n.*635T>G | |
| NM_001353200.2:c.*635T>G | NP_001340129.1:n.*635T>G | |
| NM_001374689.1:c.*635T>G | NP_001361618.1:n.*635T>G | |
| NM_001374690.1:c.*635T>G | NP_001361619.1:n.*635T>G | |
| NM_001374691.1:c.*635T>G | NP_001361620.1:n.*635T>G | |
| NM_001374692.1:c.*635T>G | NP_001361621.1:n.*635T>G | |
| NM_001374693.1:c.*635T>G | NP_001361622.1:n.*635T>G | |
| NM_001374695.1:c.*635T>G | NP_001361624.1:n.*635T>G | |
| NM_007171.4:c.*635T>G | NP_009102.4:n.*635T>G | |
| NR_148391.2:n.2671T>G | ||
| NR_148392.2:n.2889T>G | ||
| NR_148393.2:n.2986T>G | ||
| NR_148394.2:n.2740T>G | ||
| NR_148395.2:n.3138T>G | ||
| NR_148396.2:n.2772T>G | ||
| NR_148397.2:n.2897T>G | ||
| NR_148398.2:n.2852T>G | ||
| NR_148399.2:n.3202T>G | ||
| NR_148400.2:n.2977T>G |