Linked Data
ClinVar Variation Id:
387083
dbSNP Id:
rs372138410
ExAC:
6:152694166 A / G
gnomAD v2:
6-152694166-A-G
gnomAD v3:
6-152373031-A-G
gnomAD v4:
6-152373031-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152373031A>G , CM000668.2:g.152373031A>G | GRCh38 |
| NC_000006.11:g.152694166A>G , CM000668.1:g.152694166A>G | GRCh37 |
| NC_000006.10:g.152735859A>G | NCBI36 |
| NG_012855.1:g.269369T>C | |
| NG_012855.2:g.269369T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000454018.7:c.858+6T>C | ENSP00000390858.4:n.858+6T>C | |
| ENST00000367255.10:c.9507+6T>C MANE Select | ENSP00000356224.5:n.9507+6T>C | |
| ENST00000423061.6:c.9528+6T>C | ENSP00000396024.1:n.9528+6T>C | |
| ENST00000341594.9:c.9573+6T>C | ENSP00000341887.6:n.9573+6T>C | |
| ENST00000367255.9:c.9507+6T>C | ENSP00000356224.5:n.9507+6T>C | |
| ENST00000423061.5:c.9528+6T>C | ENSP00000396024.1:n.9528+6T>C | |
| ENST00000454018.6:c.855+6T>C | ENSP00000390858.3:n.855+6T>C | |
| ENST00000469439.1:c.100+6T>C | ||
| ENST00000471834.1:n.713+6T>C | ||
| NM_033071.3:c.9528+6T>C | NP_149062.1:n.9528+6T>C | |
| NM_182961.3:c.9507+6T>C | NP_892006.3:n.9507+6T>C | |
| XM_006715407.1:c.9528+6T>C | XP_006715470.1:n.9528+6T>C | |
| XM_006715408.1:c.9528+6T>C | XP_006715471.1:n.9528+6T>C | |
| XM_006715409.1:c.9507+6T>C | XP_006715472.1:n.9507+6T>C | |
| XM_006715410.1:c.9528+6T>C | XP_006715473.1:n.9528+6T>C | |
| XM_006715411.1:c.9477+6T>C | XP_006715474.1:n.9477+6T>C | |
| XM_006715412.1:c.9528+6T>C | XP_006715475.1:n.9528+6T>C | |
| XM_006715413.1:c.9528+6T>C | XP_006715476.1:n.9528+6T>C | |
| XM_006715414.1:c.9456+6T>C | XP_006715477.1:n.9456+6T>C | |
| XM_006715415.1:c.9528+6T>C | XP_006715478.1:n.9528+6T>C | |
| XM_006715416.1:c.9528+6T>C | XP_006715479.1:n.9528+6T>C | |
| XM_006715417.1:c.9528+6T>C | XP_006715480.1:n.9528+6T>C | |
| XM_006715420.1:c.9528+6T>C | XP_006715483.1:n.9528+6T>C | |
| XM_006715421.1:c.9528+6T>C | XP_006715484.1:n.9528+6T>C | |
| XM_006715422.1:c.9369+6T>C | XP_006715485.1:n.9369+6T>C | |
| XM_006715423.1:c.9528+6T>C | XP_006715486.1:n.9528+6T>C | |
| XM_006715424.1:c.9528+6T>C | XP_006715487.1:n.9528+6T>C | |
| XM_006715425.1:c.9528+6T>C | XP_006715488.1:n.9528+6T>C | |
| XM_011535641.1:c.9528+6T>C | XP_011533943.1:n.9528+6T>C | |
| XM_011535642.1:c.9528+6T>C | XP_011533944.1:n.9528+6T>C | |
| XM_011535643.1:c.9363+6T>C | XP_011533945.1:n.9363+6T>C | |
| XM_011535644.1:c.7803+6T>C | XP_011533946.1:n.7803+6T>C | |
| XM_011535645.1:c.7296+6T>C | XP_011533947.1:n.7296+6T>C | |
| XM_011535646.1:c.9528+6T>C | XP_011533948.1:n.9528+6T>C | |
| XM_011535647.1:c.2763+6T>C | XP_011533949.1:n.2763+6T>C | |
| XM_006715408.2:c.9528+6T>C | XP_006715471.1:n.9528+6T>C | |
| XM_006715410.2:c.9528+6T>C | XP_006715473.1:n.9528+6T>C | |
| XM_006715412.2:c.9528+6T>C | XP_006715475.1:n.9528+6T>C | |
| XM_006715413.2:c.9528+6T>C | XP_006715476.1:n.9528+6T>C | |
| XM_006715415.2:c.9528+6T>C | XP_006715478.1:n.9528+6T>C | |
| XM_006715416.2:c.9528+6T>C | XP_006715479.1:n.9528+6T>C | |
| XM_006715417.2:c.9528+6T>C | XP_006715480.1:n.9528+6T>C | |
| XM_006715420.2:c.9528+6T>C | XP_006715483.1:n.9528+6T>C | |
| XM_006715421.2:c.9528+6T>C | XP_006715484.1:n.9528+6T>C | |
| XM_006715423.2:c.9528+6T>C | XP_006715486.1:n.9528+6T>C | |
| XM_006715424.2:c.9528+6T>C | XP_006715487.1:n.9528+6T>C | |
| XM_006715425.2:c.9528+6T>C | XP_006715488.1:n.9528+6T>C | |
| XM_011535641.2:c.9528+6T>C | XP_011533943.1:n.9528+6T>C | |
| XM_011535642.2:c.9528+6T>C | XP_011533944.1:n.9528+6T>C | |
| XM_011535645.2:c.7296+6T>C | XP_011533947.1:n.7296+6T>C | |
| XM_017010608.1:c.9528+6T>C | XP_016866097.1:n.9528+6T>C | |
| XM_017010609.1:c.9528+6T>C | XP_016866098.1:n.9528+6T>C | |
| XM_017010610.1:c.9507+6T>C | XP_016866099.1:n.9507+6T>C | |
| XM_017010611.2:c.9501+6T>C | XP_016866100.1:n.9501+6T>C | |
| XM_017010612.1:c.9450+6T>C | XP_016866101.1:n.9450+6T>C | |
| XM_017010613.1:c.9528+6T>C | XP_016866102.1:n.9528+6T>C | |
| XM_017010614.1:c.9528+6T>C | XP_016866103.1:n.9528+6T>C | |
| XM_017010615.1:c.9528+6T>C | XP_016866104.1:n.9528+6T>C | |
| XM_017010616.1:c.9528+6T>C | XP_016866105.1:n.9528+6T>C | |
| XM_017010617.1:c.9528+6T>C | XP_016866106.1:n.9528+6T>C | |
| XM_017010618.1:c.9528+6T>C | XP_016866107.1:n.9528+6T>C | |
| XM_017010619.1:c.7803+6T>C | XP_016866108.1:n.7803+6T>C | |
| XR_001743287.1:n.10011+6T>C | ||
| NM_182961.4:c.9507+6T>C MANE Select | NP_892006.3:n.9507+6T>C | |
| NM_033071.5:c.9528+6T>C | NP_149062.2:n.9528+6T>C |