Linked Data
ClinVar Variation Id:
286002
dbSNP Id:
rs558425673
ExAC:
6:152590373 G / C
gnomAD v2:
6-152590373-G-C
gnomAD v3:
6-152269238-G-C
gnomAD v4:
6-152269238-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152269238G>C , CM000668.2:g.152269238G>C | GRCh38 |
| NC_000006.11:g.152590373G>C , CM000668.1:g.152590373G>C | GRCh37 |
| NC_000006.10:g.152632066G>C | NCBI36 |
| NG_012855.1:g.373162C>G | |
| NG_012855.2:g.373162C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367255.10:c.18622C>G MANE Select | ENSP00000356224.5:p.Gln6208Glu | |
| ENST00000423061.6:c.18409C>G | ENSP00000396024.1:p.Gln6137Glu | |
| ENST00000341594.9:c.17407C>G | ENSP00000341887.6:p.Gln5803Glu | |
| ENST00000367255.9:c.18622C>G | ENSP00000356224.5:p.Gln6208Glu | |
| ENST00000367256.9:n.2314C>G | ||
| ENST00000409694.6:n.2206C>G | ||
| ENST00000423061.5:c.18409C>G | ENSP00000396024.1:p.Gln6137Glu | |
| NM_033071.3:c.18409C>G | NP_149062.1:p.Gln6137Glu | |
| NM_182961.3:c.18622C>G | NP_892006.3:p.Gln6208Glu | |
| XM_006715407.1:c.18658C>G | XP_006715470.1:p.Gln6220Glu | |
| XM_006715408.1:c.18646C>G | XP_006715471.1:p.Gln6216Glu | |
| XM_006715409.1:c.18637C>G | XP_006715472.1:p.Gln6213Glu | |
| XM_006715410.1:c.18658C>G | XP_006715473.1:p.Gln6220Glu | |
| XM_006715411.1:c.18607C>G | XP_006715474.1:p.Gln6203Glu | |
| XM_006715412.1:c.18643C>G | XP_006715475.1:p.Gln6215Glu | |
| XM_006715413.1:c.18658C>G | XP_006715476.1:p.Gln6220Glu | |
| XM_006715414.1:c.18586C>G | XP_006715477.1:p.Gln6196Glu | |
| XM_006715415.1:c.18658C>G | XP_006715478.1:p.Gln6220Glu | |
| XM_006715416.1:c.18643C>G | XP_006715479.1:p.Gln6215Glu | |
| XM_006715417.1:c.18517C>G | XP_006715480.1:p.Gln6173Glu | |
| XM_006715420.1:c.18505C>G | XP_006715483.1:p.Gln6169Glu | |
| XM_006715421.1:c.18502C>G | XP_006715484.1:p.Gln6168Glu | |
| XM_006715422.1:c.18499C>G | XP_006715485.1:p.Gln6167Glu | |
| XM_006715423.1:c.18658C>G | XP_006715486.1:p.Gln6220Glu | |
| XM_006715424.1:c.18658C>G | XP_006715487.1:p.Gln6220Glu | |
| XM_006715425.1:c.18658C>G | XP_006715488.1:p.Gln6220Glu | |
| XM_011535641.1:c.18655C>G | XP_011533943.1:p.Gln6219Glu | |
| XM_011535642.1:c.18643C>G | XP_011533944.1:p.Gln6215Glu | |
| XM_011535643.1:c.18493C>G | XP_011533945.1:p.Gln6165Glu | |
| XM_011535644.1:c.16933C>G | XP_011533946.1:p.Gln5645Glu | |
| XM_011535645.1:c.16426C>G | XP_011533947.1:p.Gln5476Glu | |
| XM_011535646.1:c.18658C>G | XP_011533948.1:p.Gln6220Glu | |
| XM_011535647.1:c.11893C>G | XP_011533949.1:p.Gln3965Glu | |
| XM_006715408.2:c.18646C>G | XP_006715471.1:p.Gln6216Glu | |
| XM_006715410.2:c.18658C>G | XP_006715473.1:p.Gln6220Glu | |
| XM_006715412.2:c.18643C>G | XP_006715475.1:p.Gln6215Glu | |
| XM_006715413.2:c.18658C>G | XP_006715476.1:p.Gln6220Glu | |
| XM_006715415.2:c.18658C>G | XP_006715478.1:p.Gln6220Glu | |
| XM_006715416.2:c.18643C>G | XP_006715479.1:p.Gln6215Glu | |
| XM_006715417.2:c.18517C>G | XP_006715480.1:p.Gln6173Glu | |
| XM_006715420.2:c.18505C>G | XP_006715483.1:p.Gln6169Glu | |
| XM_006715421.2:c.18502C>G | XP_006715484.1:p.Gln6168Glu | |
| XM_006715423.2:c.18658C>G | XP_006715486.1:p.Gln6220Glu | |
| XM_006715424.2:c.18658C>G | XP_006715487.1:p.Gln6220Glu | |
| XM_006715425.2:c.18658C>G | XP_006715488.1:p.Gln6220Glu | |
| XM_011535641.2:c.18655C>G | XP_011533943.1:p.Gln6219Glu | |
| XM_011535642.2:c.18643C>G | XP_011533944.1:p.Gln6215Glu | |
| XM_011535645.2:c.16426C>G | XP_011533947.1:p.Gln5476Glu | |
| XM_017010608.1:c.18658C>G | XP_016866097.1:p.Gln6220Glu | |
| XM_017010609.1:c.18658C>G | XP_016866098.1:p.Gln6220Glu | |
| XM_017010610.1:c.18637C>G | XP_016866099.1:p.Gln6213Glu | |
| XM_017010611.2:c.18631C>G | XP_016866100.1:p.Gln6211Glu | |
| XM_017010612.1:c.18580C>G | XP_016866101.1:p.Gln6194Glu | |
| XM_017010613.1:c.18655C>G | XP_016866102.1:p.Gln6219Glu | |
| XM_017010614.1:c.18502C>G | XP_016866103.1:p.Gln6168Glu | |
| XM_017010615.1:c.18502C>G | XP_016866104.1:p.Gln6168Glu | |
| XM_017010616.1:c.18658C>G | XP_016866105.1:p.Gln6220Glu | |
| XM_017010617.1:c.18655C>G | XP_016866106.1:p.Gln6219Glu | |
| XM_017010618.1:c.18643C>G | XP_016866107.1:p.Gln6215Glu | |
| XM_017010619.1:c.16933C>G | XP_016866108.1:p.Gln5645Glu | |
| XR_001743287.1:n.19141C>G | ||
| NM_182961.4:c.18622C>G MANE Select | NP_892006.3:p.Gln6208Glu | |
| NM_033071.5:c.18409C>G | NP_149062.2:p.Gln6137Glu |