Linked Data
ClinVar Variation Id:
499046
dbSNP Id:
rs966425412
gnomAD v2:
6-152762361-T-A
gnomAD v3:
6-152441226-T-A
gnomAD v4:
6-152441226-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152441226T>A , CM000668.2:g.152441226T>A | GRCh38 |
| NC_000006.11:g.152762361T>A , CM000668.1:g.152762361T>A | GRCh37 |
| NC_000006.10:g.152804054T>A | NCBI36 |
| NG_012855.1:g.201174A>T | |
| NG_012855.2:g.201174A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367255.10:c.4053A>T MANE Select | ENSP00000356224.5:p.Thr1351= | |
| ENST00000423061.6:c.4074A>T | ENSP00000396024.1:p.Thr1358= | |
| ENST00000671915.1:c.1350A>T | ENSP00000500319.1:p.Thr450= | |
| ENST00000672122.1:c.3996A>T | ENSP00000500559.1:p.Thr1332= | |
| ENST00000673163.1:c.*4023A>T | ENSP00000499934.1:n.*4023A>T | |
| ENST00000673281.1:c.4047A>T | ENSP00000500893.1:p.Thr1349= | |
| ENST00000341594.9:c.4200A>T | ENSP00000341887.6:p.Thr1400= | |
| ENST00000367248.7:c.4023A>T | ENSP00000356217.3:p.Thr1341= | |
| ENST00000367253.8:c.4053A>T | ENSP00000356222.4:p.Thr1351= | |
| ENST00000367255.9:c.4053A>T | ENSP00000356224.5:p.Thr1351= | |
| ENST00000413186.6:c.4053A>T | ENSP00000414510.2:p.Thr1351= | |
| ENST00000423061.5:c.4074A>T | ENSP00000396024.1:p.Thr1358= | |
| ENST00000461872.6:n.4271A>T | ||
| NM_033071.3:c.4074A>T | NP_149062.1:p.Thr1358= | |
| NM_182961.3:c.4053A>T | NP_892006.3:p.Thr1351= | |
| XM_006715407.1:c.4074A>T | XP_006715470.1:p.Thr1358= | |
| XM_006715408.1:c.4074A>T | XP_006715471.1:p.Thr1358= | |
| XM_006715409.1:c.4053A>T | XP_006715472.1:p.Thr1351= | |
| XM_006715410.1:c.4074A>T | XP_006715473.1:p.Thr1358= | |
| XM_006715411.1:c.4023A>T | XP_006715474.1:p.Thr1341= | |
| XM_006715412.1:c.4074A>T | XP_006715475.1:p.Thr1358= | |
| XM_006715413.1:c.4074A>T | XP_006715476.1:p.Thr1358= | |
| XM_006715414.1:c.4002A>T | XP_006715477.1:p.Thr1334= | |
| XM_006715415.1:c.4074A>T | XP_006715478.1:p.Thr1358= | |
| XM_006715416.1:c.4074A>T | XP_006715479.1:p.Thr1358= | |
| XM_006715417.1:c.4074A>T | XP_006715480.1:p.Thr1358= | |
| XM_006715420.1:c.4074A>T | XP_006715483.1:p.Thr1358= | |
| XM_006715421.1:c.4074A>T | XP_006715484.1:p.Thr1358= | |
| XM_006715422.1:c.3915A>T | XP_006715485.1:p.Thr1305= | |
| XM_006715423.1:c.4074A>T | XP_006715486.1:p.Thr1358= | |
| XM_006715424.1:c.4074A>T | XP_006715487.1:p.Thr1358= | |
| XM_006715425.1:c.4074A>T | XP_006715488.1:p.Thr1358= | |
| XM_011535641.1:c.4074A>T | XP_011533943.1:p.Thr1358= | |
| XM_011535642.1:c.4074A>T | XP_011533944.1:p.Thr1358= | |
| XM_011535643.1:c.3909A>T | XP_011533945.1:p.Thr1303= | |
| XM_011535644.1:c.2349A>T | XP_011533946.1:p.Thr783= | |
| XM_011535645.1:c.1842A>T | XP_011533947.1:p.Thr614= | |
| XM_011535646.1:c.4074A>T | XP_011533948.1:p.Thr1358= | |
| XM_006715408.2:c.4074A>T | XP_006715471.1:p.Thr1358= | |
| XM_006715410.2:c.4074A>T | XP_006715473.1:p.Thr1358= | |
| XM_006715412.2:c.4074A>T | XP_006715475.1:p.Thr1358= | |
| XM_006715413.2:c.4074A>T | XP_006715476.1:p.Thr1358= | |
| XM_006715415.2:c.4074A>T | XP_006715478.1:p.Thr1358= | |
| XM_006715416.2:c.4074A>T | XP_006715479.1:p.Thr1358= | |
| XM_006715417.2:c.4074A>T | XP_006715480.1:p.Thr1358= | |
| XM_006715420.2:c.4074A>T | XP_006715483.1:p.Thr1358= | |
| XM_006715421.2:c.4074A>T | XP_006715484.1:p.Thr1358= | |
| XM_006715423.2:c.4074A>T | XP_006715486.1:p.Thr1358= | |
| XM_006715424.2:c.4074A>T | XP_006715487.1:p.Thr1358= | |
| XM_006715425.2:c.4074A>T | XP_006715488.1:p.Thr1358= | |
| XM_011535641.2:c.4074A>T | XP_011533943.1:p.Thr1358= | |
| XM_011535642.2:c.4074A>T | XP_011533944.1:p.Thr1358= | |
| XM_011535645.2:c.1842A>T | XP_011533947.1:p.Thr614= | |
| XM_017010608.1:c.4074A>T | XP_016866097.1:p.Thr1358= | |
| XM_017010609.1:c.4074A>T | XP_016866098.1:p.Thr1358= | |
| XM_017010610.1:c.4053A>T | XP_016866099.1:p.Thr1351= | |
| XM_017010611.2:c.4047A>T | XP_016866100.1:p.Thr1349= | |
| XM_017010612.1:c.3996A>T | XP_016866101.1:p.Thr1332= | |
| XM_017010613.1:c.4074A>T | XP_016866102.1:p.Thr1358= | |
| XM_017010614.1:c.4074A>T | XP_016866103.1:p.Thr1358= | |
| XM_017010615.1:c.4074A>T | XP_016866104.1:p.Thr1358= | |
| XM_017010616.1:c.4074A>T | XP_016866105.1:p.Thr1358= | |
| XM_017010617.1:c.4074A>T | XP_016866106.1:p.Thr1358= | |
| XM_017010618.1:c.4074A>T | XP_016866107.1:p.Thr1358= | |
| XM_017010619.1:c.2349A>T | XP_016866108.1:p.Thr783= | |
| XR_001743287.1:n.4557A>T | ||
| NM_182961.4:c.4053A>T MANE Select | NP_892006.3:p.Thr1351= | |
| NM_033071.5:c.4074A>T | NP_149062.2:p.Thr1358= |