Linked Data
ClinVar Variation Id:
448543
dbSNP Id:
rs138882800
ExAC:
6:152674404 C / T
gnomAD v2:
6-152674404-C-T
gnomAD v3:
6-152353269-C-T
gnomAD v4:
6-152353269-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152353269C>T , CM000668.2:g.152353269C>T | GRCh38 |
| NC_000006.11:g.152674404C>T , CM000668.1:g.152674404C>T | GRCh37 |
| NC_000006.10:g.152716097C>T | NCBI36 |
| NG_012855.1:g.289131G>A | |
| NG_012855.2:g.289131G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367255.10:c.11247G>A MANE Select | ENSP00000356224.5:p.Thr3749= | |
| ENST00000423061.6:c.11202G>A | ENSP00000396024.1:p.Thr3734= | |
| ENST00000341594.9:c.11109G>A | ENSP00000341887.6:p.Thr3703= | |
| ENST00000367255.9:c.11247G>A | ENSP00000356224.5:p.Thr3749= | |
| ENST00000423061.5:c.11202G>A | ENSP00000396024.1:p.Thr3734= | |
| ENST00000471834.1:n.4385G>A | ||
| NM_033071.3:c.11202G>A | NP_149062.1:p.Thr3734= | |
| NM_182961.3:c.11247G>A | NP_892006.3:p.Thr3749= | |
| XM_006715407.1:c.11268G>A | XP_006715470.1:p.Thr3756= | |
| XM_006715408.1:c.11268G>A | XP_006715471.1:p.Thr3756= | |
| XM_006715409.1:c.11247G>A | XP_006715472.1:p.Thr3749= | |
| XM_006715410.1:c.11268G>A | XP_006715473.1:p.Thr3756= | |
| XM_006715411.1:c.11217G>A | XP_006715474.1:p.Thr3739= | |
| XM_006715412.1:c.11268G>A | XP_006715475.1:p.Thr3756= | |
| XM_006715413.1:c.11268G>A | XP_006715476.1:p.Thr3756= | |
| XM_006715414.1:c.11196G>A | XP_006715477.1:p.Thr3732= | |
| XM_006715415.1:c.11268G>A | XP_006715478.1:p.Thr3756= | |
| XM_006715416.1:c.11268G>A | XP_006715479.1:p.Thr3756= | |
| XM_006715417.1:c.11268G>A | XP_006715480.1:p.Thr3756= | |
| XM_006715420.1:c.11268G>A | XP_006715483.1:p.Thr3756= | |
| XM_006715421.1:c.11112G>A | XP_006715484.1:p.Thr3704= | |
| XM_006715422.1:c.11109G>A | XP_006715485.1:p.Thr3703= | |
| XM_006715423.1:c.11268G>A | XP_006715486.1:p.Thr3756= | |
| XM_006715424.1:c.11268G>A | XP_006715487.1:p.Thr3756= | |
| XM_006715425.1:c.11268G>A | XP_006715488.1:p.Thr3756= | |
| XM_011535641.1:c.11268G>A | XP_011533943.1:p.Thr3756= | |
| XM_011535642.1:c.11268G>A | XP_011533944.1:p.Thr3756= | |
| XM_011535643.1:c.11103G>A | XP_011533945.1:p.Thr3701= | |
| XM_011535644.1:c.9543G>A | XP_011533946.1:p.Thr3181= | |
| XM_011535645.1:c.9036G>A | XP_011533947.1:p.Thr3012= | |
| XM_011535646.1:c.11268G>A | XP_011533948.1:p.Thr3756= | |
| XM_011535647.1:c.4503G>A | XP_011533949.1:p.Thr1501= | |
| XM_006715408.2:c.11268G>A | XP_006715471.1:p.Thr3756= | |
| XM_006715410.2:c.11268G>A | XP_006715473.1:p.Thr3756= | |
| XM_006715412.2:c.11268G>A | XP_006715475.1:p.Thr3756= | |
| XM_006715413.2:c.11268G>A | XP_006715476.1:p.Thr3756= | |
| XM_006715415.2:c.11268G>A | XP_006715478.1:p.Thr3756= | |
| XM_006715416.2:c.11268G>A | XP_006715479.1:p.Thr3756= | |
| XM_006715417.2:c.11268G>A | XP_006715480.1:p.Thr3756= | |
| XM_006715420.2:c.11268G>A | XP_006715483.1:p.Thr3756= | |
| XM_006715421.2:c.11112G>A | XP_006715484.1:p.Thr3704= | |
| XM_006715423.2:c.11268G>A | XP_006715486.1:p.Thr3756= | |
| XM_006715424.2:c.11268G>A | XP_006715487.1:p.Thr3756= | |
| XM_006715425.2:c.11268G>A | XP_006715488.1:p.Thr3756= | |
| XM_011535641.2:c.11268G>A | XP_011533943.1:p.Thr3756= | |
| XM_011535642.2:c.11268G>A | XP_011533944.1:p.Thr3756= | |
| XM_011535645.2:c.9036G>A | XP_011533947.1:p.Thr3012= | |
| XM_017010608.1:c.11268G>A | XP_016866097.1:p.Thr3756= | |
| XM_017010609.1:c.11268G>A | XP_016866098.1:p.Thr3756= | |
| XM_017010610.1:c.11247G>A | XP_016866099.1:p.Thr3749= | |
| XM_017010611.2:c.11241G>A | XP_016866100.1:p.Thr3747= | |
| XM_017010612.1:c.11190G>A | XP_016866101.1:p.Thr3730= | |
| XM_017010613.1:c.11268G>A | XP_016866102.1:p.Thr3756= | |
| XM_017010614.1:c.11268G>A | XP_016866103.1:p.Thr3756= | |
| XM_017010615.1:c.11268G>A | XP_016866104.1:p.Thr3756= | |
| XM_017010616.1:c.11268G>A | XP_016866105.1:p.Thr3756= | |
| XM_017010617.1:c.11268G>A | XP_016866106.1:p.Thr3756= | |
| XM_017010618.1:c.11268G>A | XP_016866107.1:p.Thr3756= | |
| XM_017010619.1:c.9543G>A | XP_016866108.1:p.Thr3181= | |
| XR_001743287.1:n.11751G>A | ||
| NM_182961.4:c.11247G>A MANE Select | NP_892006.3:p.Thr3749= | |
| NM_033071.5:c.11202G>A | NP_149062.2:p.Thr3734= |