Linked Data
ClinVar Variation Id:
510992
dbSNP Id:
rs1020832262
gnomAD v2:
6-152694175-T-C
gnomAD v3:
6-152373040-T-C
gnomAD v4:
6-152373040-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152373040T>C , CM000668.2:g.152373040T>C | GRCh38 |
| NC_000006.11:g.152694175T>C , CM000668.1:g.152694175T>C | GRCh37 |
| NC_000006.10:g.152735868T>C | NCBI36 |
| NG_012855.1:g.269360A>G | |
| NG_012855.2:g.269360A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000454018.7:c.855A>G | ENSP00000390858.4:p.Leu285= | |
| ENST00000367255.10:c.9504A>G MANE Select | ENSP00000356224.5:p.Leu3168= | |
| ENST00000423061.6:c.9525A>G | ENSP00000396024.1:p.Leu3175= | |
| ENST00000341594.9:c.9570A>G | ENSP00000341887.6:p.Leu3190= | |
| ENST00000367255.9:c.9504A>G | ENSP00000356224.5:p.Leu3168= | |
| ENST00000423061.5:c.9525A>G | ENSP00000396024.1:p.Leu3175= | |
| ENST00000454018.6:c.852A>G | ENSP00000390858.3:p.Leu284= | |
| ENST00000469439.1:c.97A>G | ||
| ENST00000471834.1:n.710A>G | ||
| NM_033071.3:c.9525A>G | NP_149062.1:p.Leu3175= | |
| NM_182961.3:c.9504A>G | NP_892006.3:p.Leu3168= | |
| XM_006715407.1:c.9525A>G | XP_006715470.1:p.Leu3175= | |
| XM_006715408.1:c.9525A>G | XP_006715471.1:p.Leu3175= | |
| XM_006715409.1:c.9504A>G | XP_006715472.1:p.Leu3168= | |
| XM_006715410.1:c.9525A>G | XP_006715473.1:p.Leu3175= | |
| XM_006715411.1:c.9474A>G | XP_006715474.1:p.Leu3158= | |
| XM_006715412.1:c.9525A>G | XP_006715475.1:p.Leu3175= | |
| XM_006715413.1:c.9525A>G | XP_006715476.1:p.Leu3175= | |
| XM_006715414.1:c.9453A>G | XP_006715477.1:p.Leu3151= | |
| XM_006715415.1:c.9525A>G | XP_006715478.1:p.Leu3175= | |
| XM_006715416.1:c.9525A>G | XP_006715479.1:p.Leu3175= | |
| XM_006715417.1:c.9525A>G | XP_006715480.1:p.Leu3175= | |
| XM_006715420.1:c.9525A>G | XP_006715483.1:p.Leu3175= | |
| XM_006715421.1:c.9525A>G | XP_006715484.1:p.Leu3175= | |
| XM_006715422.1:c.9366A>G | XP_006715485.1:p.Leu3122= | |
| XM_006715423.1:c.9525A>G | XP_006715486.1:p.Leu3175= | |
| XM_006715424.1:c.9525A>G | XP_006715487.1:p.Leu3175= | |
| XM_006715425.1:c.9525A>G | XP_006715488.1:p.Leu3175= | |
| XM_011535641.1:c.9525A>G | XP_011533943.1:p.Leu3175= | |
| XM_011535642.1:c.9525A>G | XP_011533944.1:p.Leu3175= | |
| XM_011535643.1:c.9360A>G | XP_011533945.1:p.Leu3120= | |
| XM_011535644.1:c.7800A>G | XP_011533946.1:p.Leu2600= | |
| XM_011535645.1:c.7293A>G | XP_011533947.1:p.Leu2431= | |
| XM_011535646.1:c.9525A>G | XP_011533948.1:p.Leu3175= | |
| XM_011535647.1:c.2760A>G | XP_011533949.1:p.Leu920= | |
| XM_006715408.2:c.9525A>G | XP_006715471.1:p.Leu3175= | |
| XM_006715410.2:c.9525A>G | XP_006715473.1:p.Leu3175= | |
| XM_006715412.2:c.9525A>G | XP_006715475.1:p.Leu3175= | |
| XM_006715413.2:c.9525A>G | XP_006715476.1:p.Leu3175= | |
| XM_006715415.2:c.9525A>G | XP_006715478.1:p.Leu3175= | |
| XM_006715416.2:c.9525A>G | XP_006715479.1:p.Leu3175= | |
| XM_006715417.2:c.9525A>G | XP_006715480.1:p.Leu3175= | |
| XM_006715420.2:c.9525A>G | XP_006715483.1:p.Leu3175= | |
| XM_006715421.2:c.9525A>G | XP_006715484.1:p.Leu3175= | |
| XM_006715423.2:c.9525A>G | XP_006715486.1:p.Leu3175= | |
| XM_006715424.2:c.9525A>G | XP_006715487.1:p.Leu3175= | |
| XM_006715425.2:c.9525A>G | XP_006715488.1:p.Leu3175= | |
| XM_011535641.2:c.9525A>G | XP_011533943.1:p.Leu3175= | |
| XM_011535642.2:c.9525A>G | XP_011533944.1:p.Leu3175= | |
| XM_011535645.2:c.7293A>G | XP_011533947.1:p.Leu2431= | |
| XM_017010608.1:c.9525A>G | XP_016866097.1:p.Leu3175= | |
| XM_017010609.1:c.9525A>G | XP_016866098.1:p.Leu3175= | |
| XM_017010610.1:c.9504A>G | XP_016866099.1:p.Leu3168= | |
| XM_017010611.2:c.9498A>G | XP_016866100.1:p.Leu3166= | |
| XM_017010612.1:c.9447A>G | XP_016866101.1:p.Leu3149= | |
| XM_017010613.1:c.9525A>G | XP_016866102.1:p.Leu3175= | |
| XM_017010614.1:c.9525A>G | XP_016866103.1:p.Leu3175= | |
| XM_017010615.1:c.9525A>G | XP_016866104.1:p.Leu3175= | |
| XM_017010616.1:c.9525A>G | XP_016866105.1:p.Leu3175= | |
| XM_017010617.1:c.9525A>G | XP_016866106.1:p.Leu3175= | |
| XM_017010618.1:c.9525A>G | XP_016866107.1:p.Leu3175= | |
| XM_017010619.1:c.7800A>G | XP_016866108.1:p.Leu2600= | |
| XR_001743287.1:n.10008A>G | ||
| NM_182961.4:c.9504A>G MANE Select | NP_892006.3:p.Leu3168= | |
| NM_033071.5:c.9525A>G | NP_149062.2:p.Leu3175= |