Linked Data
ClinVar Variation Id:
318326
dbSNP Id:
rs539927192
ExAC:
16:2129355 G / A
gnomAD v2:
16-2129355-G-A
gnomAD v3:
16-2079354-G-A
gnomAD v4:
16-2079354-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2079354G>A , CM000678.2:g.2079354G>A | GRCh38 |
| NC_000016.9:g.2129355G>A , CM000678.1:g.2129355G>A | GRCh37 |
| NC_000016.8:g.2069356G>A | NCBI36 |
| NG_005895.1:g.35049G>A , LRG_487:g.35049G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*1628G>A | ENSP00000455997.2:n.*1628G>A | |
| ENST00000642206.2:c.3126G>A | ENSP00000495146.2:p.Thr1042= | |
| ENST00000642365.2:c.3207G>A | ENSP00000495459.2:p.Thr1069= | |
| ENST00000644417.2:c.*3659G>A | ENSP00000493912.2:n.*3659G>A | |
| ENST00000646464.2:c.*4132G>A | ENSP00000496610.2:n.*4132G>A | |
| ENST00000219476.9:c.3210G>A MANE Select | ENSP00000219476.3:p.Thr1070= | |
| ENST00000350773.9:c.3210G>A | ENSP00000344383.4:p.Thr1070= | |
| ENST00000401874.7:c.3078G>A | ENSP00000384468.2:p.Thr1026= | |
| ENST00000471143.6:c.438G>A | ENSP00000458541.2:n.438G>A | |
| ENST00000568454.6:c.3111G>A | ENSP00000454487.1:p.Thr1037= | |
| ENST00000642365.1:c.1864G>A | ||
| ENST00000642561.1:c.3081G>A | ENSP00000495099.1:p.Thr1027= | |
| ENST00000642797.1:c.3081G>A | ENSP00000493846.1:p.Thr1027= | |
| ENST00000642936.1:c.3078G>A | ENSP00000494514.1:p.Thr1026= | |
| ENST00000643088.1:c.3078G>A | ENSP00000494747.1:p.Thr1026= | |
| ENST00000643946.1:c.3210G>A | ENSP00000495927.1:p.Thr1070= | |
| ENST00000644043.1:c.3081G>A | ENSP00000496262.1:p.Thr1027= | |
| ENST00000644329.1:c.3078G>A | ENSP00000496611.1:p.Thr1026= | |
| ENST00000644335.1:c.3081G>A | ENSP00000496317.1:p.Thr1027= | |
| ENST00000644399.1:c.3200G>A | ||
| ENST00000644722.1:n.356G>A | ||
| ENST00000645024.1:n.1363G>A | ||
| ENST00000646388.1:c.3210G>A | ENSP00000495921.1:p.Thr1070= | |
| ENST00000646634.1:n.2094G>A | ||
| ENST00000647042.1:n.502G>A | ||
| ENST00000219476.7:c.3210G>A | ENSP00000219476.3:p.Thr1070= | |
| ENST00000350773.8:c.3210G>A | ENSP00000344383.4:p.Thr1070= | |
| ENST00000382538.10:c.2934G>A | ENSP00000371978.6:p.Thr978= | |
| ENST00000401874.6:c.3078G>A | ENSP00000384468.2:p.Thr1026= | |
| ENST00000439117.6:c.*2377G>A | ENSP00000406980.2:n.*2377G>A | |
| ENST00000439673.6:c.2970G>A | ENSP00000399232.2:p.Thr990= | |
| ENST00000471143.5:c.436G>A | ||
| ENST00000483020.5:c.450G>A | ENSP00000460310.1:n.450G>A | |
| ENST00000497886.5:n.1037G>A | ||
| ENST00000561695.1:n.435G>A | ||
| ENST00000568366.5:n.567G>A | ||
| ENST00000568454.5:c.3111G>A | ENSP00000454487.1:p.Thr1037= | |
| NM_000548.3:c.3210G>A , LRG_487t1:c.3210G>A | NP_000539.2:p.Thr1070= | |
| NM_001077183.1:c.3078G>A | NP_001070651.1:p.Thr1026= | |
| NM_001114382.1:c.3210G>A | NP_001107854.1:p.Thr1070= | |
| XM_005255529.3:c.3081G>A | XP_005255586.2:p.Thr1027= | |
| XM_005255531.3:c.3081G>A | XP_005255588.2:p.Thr1027= | |
| XM_011522636.1:c.3210G>A | XP_011520938.1:p.Thr1070= | |
| XM_011522637.1:c.3207G>A | XP_011520939.1:p.Thr1069= | |
| XM_011522638.1:c.3099G>A | XP_011520940.1:p.Thr1033= | |
| XM_011522639.1:c.3081G>A | XP_011520941.1:p.Thr1027= | |
| XM_011522640.1:c.3078G>A | XP_011520942.1:p.Thr1026= | |
| XM_011522641.1:c.2970G>A | XP_011520943.1:p.Thr990= | |
| NM_000548.4:c.3210G>A | NP_000539.2:p.Thr1070= | |
| NM_001077183.2:c.3078G>A | NP_001070651.1:p.Thr1026= | |
| NM_001114382.2:c.3210G>A | NP_001107854.1:p.Thr1070= | |
| NM_001318827.1:c.2970G>A | NP_001305756.1:p.Thr990= | |
| NM_001318829.1:c.2934G>A | NP_001305758.1:p.Thr978= | |
| NM_001318831.1:c.2478G>A | NP_001305760.1:p.Thr826= | |
| NM_001318832.1:c.3111G>A | NP_001305761.1:p.Thr1037= | |
| NM_001363528.1:c.3081G>A | NP_001350457.1:p.Thr1027= | |
| NM_021055.2:c.3081G>A | NP_066399.2:p.Thr1027= | |
| XM_005255531.4:c.3081G>A | XP_005255588.2:p.Thr1027= | |
| XM_011522636.2:c.3210G>A | XP_011520938.1:p.Thr1070= | |
| XM_011522637.2:c.3207G>A | XP_011520939.1:p.Thr1069= | |
| XM_011522638.2:c.3372G>A | XP_011520940.2:p.Thr1124= | |
| XM_011522639.2:c.3081G>A | XP_011520941.1:p.Thr1027= | |
| XM_011522640.2:c.3078G>A | XP_011520942.1:p.Thr1026= | |
| XM_017023615.1:c.3207G>A | XP_016879104.1:p.Thr1069= | |
| XM_017023616.1:c.3078G>A | XP_016879105.1:p.Thr1026= | |
| XM_017023617.1:c.3243G>A | XP_016879106.1:p.Thr1081= | |
| XM_017023618.1:c.1866G>A | XP_016879107.1:p.Thr622= | |
| XM_024450413.1:c.3078G>A | XP_024306181.1:p.Thr1026= | |
| NM_000548.5:c.3210G>A MANE Select | NP_000539.2:p.Thr1070= | |
| NM_001370404.1:c.3078G>A | NP_001357333.1:p.Thr1026= | |
| NM_001370405.1:c.3081G>A | NP_001357334.1:p.Thr1027= | |
| NM_001077183.3:c.3078G>A | NP_001070651.1:p.Thr1026= | |
| NM_001114382.3:c.3210G>A | NP_001107854.1:p.Thr1070= | |
| NM_001318827.2:c.2970G>A | NP_001305756.1:p.Thr990= | |
| NM_001318829.2:c.2934G>A | NP_001305758.1:p.Thr978= | |
| NM_001318831.2:c.2478G>A | NP_001305760.1:p.Thr826= | |
| NM_001318832.2:c.3111G>A | NP_001305761.1:p.Thr1037= | |
| NM_001363528.2:c.3081G>A | NP_001350457.1:p.Thr1027= | |
| NM_021055.3:c.3081G>A | NP_066399.2:p.Thr1027= |