Linked Data
ClinVar Variation Id:
501560
dbSNP Id:
rs750669148
ExAC:
6:152540147 A / C
gnomAD v2:
6-152540147-A-C
gnomAD v3:
6-152219012-A-C
gnomAD v4:
6-152219012-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152219012A>C , CM000668.2:g.152219012A>C | GRCh38 |
| NC_000006.11:g.152540147A>C , CM000668.1:g.152540147A>C | GRCh37 |
| NC_000006.10:g.152581840A>C | NCBI36 |
| NG_012855.1:g.423388T>G | |
| NG_012855.2:g.423388T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367255.10:c.22035T>G MANE Select | ENSP00000356224.5:p.Thr7345= | |
| ENST00000423061.6:c.21822T>G | ENSP00000396024.1:p.Thr7274= | |
| ENST00000341594.9:c.20820T>G | ENSP00000341887.6:p.Thr6940= | |
| ENST00000367251.7:c.801T>G | ENSP00000356220.3:p.Thr267= | |
| ENST00000367255.9:c.22035T>G | ENSP00000356224.5:p.Thr7345= | |
| ENST00000367256.9:n.5727T>G | ||
| ENST00000409694.6:n.5619T>G | ||
| ENST00000423061.5:c.21822T>G | ENSP00000396024.1:p.Thr7274= | |
| NM_033071.3:c.21822T>G | NP_149062.1:p.Thr7274= | |
| NM_182961.3:c.22035T>G | NP_892006.3:p.Thr7345= | |
| XM_006715407.1:c.22071T>G | XP_006715470.1:p.Thr7357= | |
| XM_006715408.1:c.22059T>G | XP_006715471.1:p.Thr7353= | |
| XM_006715409.1:c.22050T>G | XP_006715472.1:p.Thr7350= | |
| XM_006715410.1:c.22071T>G | XP_006715473.1:p.Thr7357= | |
| XM_006715411.1:c.22020T>G | XP_006715474.1:p.Thr7340= | |
| XM_006715412.1:c.22056T>G | XP_006715475.1:p.Thr7352= | |
| XM_006715413.1:c.22071T>G | XP_006715476.1:p.Thr7357= | |
| XM_006715414.1:c.21999T>G | XP_006715477.1:p.Thr7333= | |
| XM_006715415.1:c.22071T>G | XP_006715478.1:p.Thr7357= | |
| XM_006715416.1:c.22056T>G | XP_006715479.1:p.Thr7352= | |
| XM_006715417.1:c.21930T>G | XP_006715480.1:p.Thr7310= | |
| XM_006715420.1:c.21918T>G | XP_006715483.1:p.Thr7306= | |
| XM_006715421.1:c.21915T>G | XP_006715484.1:p.Thr7305= | |
| XM_006715422.1:c.21912T>G | XP_006715485.1:p.Thr7304= | |
| XM_006715423.1:c.22071T>G | XP_006715486.1:p.Thr7357= | |
| XM_006715424.1:c.22071T>G | XP_006715487.1:p.Thr7357= | |
| XM_006715425.1:c.22071T>G | XP_006715488.1:p.Thr7357= | |
| XM_011535641.1:c.22068T>G | XP_011533943.1:p.Thr7356= | |
| XM_011535642.1:c.22056T>G | XP_011533944.1:p.Thr7352= | |
| XM_011535643.1:c.21906T>G | XP_011533945.1:p.Thr7302= | |
| XM_011535644.1:c.20346T>G | XP_011533946.1:p.Thr6782= | |
| XM_011535645.1:c.19839T>G | XP_011533947.1:p.Thr6613= | |
| XM_011535647.1:c.15306T>G | XP_011533949.1:p.Thr5102= | |
| XM_006715408.2:c.22059T>G | XP_006715471.1:p.Thr7353= | |
| XM_006715410.2:c.22071T>G | XP_006715473.1:p.Thr7357= | |
| XM_006715412.2:c.22056T>G | XP_006715475.1:p.Thr7352= | |
| XM_006715413.2:c.22071T>G | XP_006715476.1:p.Thr7357= | |
| XM_006715415.2:c.22071T>G | XP_006715478.1:p.Thr7357= | |
| XM_006715416.2:c.22056T>G | XP_006715479.1:p.Thr7352= | |
| XM_006715417.2:c.21930T>G | XP_006715480.1:p.Thr7310= | |
| XM_006715420.2:c.21918T>G | XP_006715483.1:p.Thr7306= | |
| XM_006715421.2:c.21915T>G | XP_006715484.1:p.Thr7305= | |
| XM_006715423.2:c.22071T>G | XP_006715486.1:p.Thr7357= | |
| XM_006715424.2:c.22071T>G | XP_006715487.1:p.Thr7357= | |
| XM_006715425.2:c.22071T>G | XP_006715488.1:p.Thr7357= | |
| XM_011535641.2:c.22068T>G | XP_011533943.1:p.Thr7356= | |
| XM_011535642.2:c.22056T>G | XP_011533944.1:p.Thr7352= | |
| XM_011535645.2:c.19839T>G | XP_011533947.1:p.Thr6613= | |
| XM_017010608.1:c.22071T>G | XP_016866097.1:p.Thr7357= | |
| XM_017010609.1:c.22071T>G | XP_016866098.1:p.Thr7357= | |
| XM_017010610.1:c.22050T>G | XP_016866099.1:p.Thr7350= | |
| XM_017010611.2:c.22044T>G | XP_016866100.1:p.Thr7348= | |
| XM_017010612.1:c.21993T>G | XP_016866101.1:p.Thr7331= | |
| XM_017010613.1:c.22068T>G | XP_016866102.1:p.Thr7356= | |
| XM_017010614.1:c.21915T>G | XP_016866103.1:p.Thr7305= | |
| XM_017010615.1:c.21915T>G | XP_016866104.1:p.Thr7305= | |
| XM_017010616.1:c.22071T>G | XP_016866105.1:p.Thr7357= | |
| XM_017010617.1:c.22068T>G | XP_016866106.1:p.Thr7356= | |
| XM_017010618.1:c.22056T>G | XP_016866107.1:p.Thr7352= | |
| XM_017010619.1:c.20346T>G | XP_016866108.1:p.Thr6782= | |
| NM_182961.4:c.22035T>G MANE Select | NP_892006.3:p.Thr7345= | |
| NM_033071.5:c.21822T>G | NP_149062.2:p.Thr7274= |