Linked Data
ClinVar Variation Id:
178483
dbSNP Id:
rs60103800
gnomAD v3:
11-77182132-A-G
gnomAD v4:
11-77182132-A-G
MyVariant Identifiers:
chr11:g.77182132A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.77182132A>G , CM000673.2:g.77182132A>G | GRCh38 |
| NC_000011.8:g.76570826A>G | NCBI36 |
| NG_009086.1:g.58869A>G | |
| NG_009086.2:g.58887A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000409709.9:c.3086A>G MANE Select | ENSP00000386331.3:p.His1029Arg | |
| ENST00000409893.6:c.1151A>G | ENSP00000386689.2:p.His384Arg | |
| ENST00000670577.1:c.927A>G | ||
| ENST00000409619.6:c.3053A>G | ENSP00000386635.2:p.His1018Arg | |
| ENST00000409709.7:c.3086A>G | ENSP00000386331.3:p.His1029Arg | |
| ENST00000409893.5:c.3086A>G | ENSP00000386689.1:p.His1029Arg | |
| ENST00000458169.2:c.629A>G | ENSP00000417017.2:p.His210Arg | |
| ENST00000458637.6:c.3086A>G | ENSP00000392185.2:p.His1029Arg | |
| ENST00000481328.7:n.629A>G | ||
| ENST00000620575.4:c.3086A>G | ENSP00000477640.1:p.His1029Arg | |
| NM_000260.3:c.3086A>G | NP_000251.3:p.His1029Arg | |
| NM_001127179.2:c.3086A>G | NP_001120651.2:p.His1029Arg | |
| NM_001127180.1:c.3086A>G | NP_001120652.1:p.His1029Arg | |
| XM_005274012.2:c.3086A>G | XP_005274069.1:p.His1029Arg | |
| XM_006718558.2:c.3086A>G | XP_006718621.1:p.His1029Arg | |
| XM_006718559.2:c.3086A>G | XP_006718622.1:p.His1029Arg | |
| XM_006718560.2:c.3086A>G | XP_006718623.1:p.His1029Arg | |
| XM_006718561.2:c.3086A>G | XP_006718624.1:p.His1029Arg | |
| XM_011545044.1:c.3086A>G | XP_011543346.1:p.His1029Arg | |
| XM_011545045.1:c.3086A>G | XP_011543347.1:p.His1029Arg | |
| XM_011545046.1:c.3053A>G | XP_011543348.1:p.His1018Arg | |
| XM_011545047.1:c.3086A>G | XP_011543349.1:p.His1029Arg | |
| XM_011545048.1:c.2867A>G | XP_011543350.1:p.His956Arg | |
| XM_011545049.1:c.2855A>G | XP_011543351.1:p.His952Arg | |
| XM_011545050.1:c.2828A>G | XP_011543352.1:p.His943Arg | |
| XM_011545051.1:c.3086A>G | XP_011543353.1:p.His1029Arg | |
| XM_011545052.1:c.3086A>G | XP_011543354.1:p.His1029Arg | |
| XR_949938.1:n.3406A>G | ||
| XR_949941.1:n.3406A>G | ||
| XR_949942.1:n.3408A>G | ||
| XR_949943.1:n.3408A>G | ||
| XM_011545044.2:c.3086A>G | XP_011543346.1:p.His1029Arg | |
| XM_011545046.2:c.3176A>G | XP_011543348.2:p.His1059Arg | |
| XM_011545050.2:c.2828A>G | XP_011543352.1:p.His943Arg | |
| XM_017017778.1:c.3176A>G | XP_016873267.1:p.His1059Arg | |
| XM_017017779.1:c.3176A>G | XP_016873268.1:p.His1059Arg | |
| XM_017017780.1:c.3176A>G | XP_016873269.1:p.His1059Arg | |
| XM_017017781.1:c.3176A>G | XP_016873270.1:p.His1059Arg | |
| XM_017017782.1:c.3176A>G | XP_016873271.1:p.His1059Arg | |
| XM_017017783.1:c.3176A>G | XP_016873272.1:p.His1059Arg | |
| XM_017017784.1:c.3176A>G | XP_016873273.1:p.His1059Arg | |
| XM_017017785.1:c.2945A>G | XP_016873274.1:p.His982Arg | |
| XM_017017786.1:c.3176A>G | XP_016873275.1:p.His1059Arg | |
| XM_017017787.1:c.3176A>G | XP_016873276.1:p.His1059Arg | |
| XM_017017788.1:c.3176A>G | XP_016873277.1:p.His1059Arg | |
| XR_001747885.1:n.3191A>G | ||
| XR_001747886.1:n.3191A>G | ||
| XR_001747887.1:n.3191A>G | ||
| XR_001747888.1:n.3191A>G | ||
| XR_001747889.1:n.3191A>G | ||
| NM_000260.4:c.3086A>G MANE Select | NP_000251.3:p.His1029Arg | |
| NM_001127180.2:c.3086A>G | NP_001120652.1:p.His1029Arg | |
| NM_001369365.1:c.3053A>G | NP_001356294.1:p.His1018Arg |