Linked Data
ClinVar Variation Id:
283627
dbSNP Id:
rs117346210
ExAC:
6:152470609 T / C
gnomAD v2:
6-152470609-T-C
gnomAD v3:
6-152149474-T-C
gnomAD v4:
6-152149474-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152149474T>C , CM000668.2:g.152149474T>C | GRCh38 |
| NC_000006.11:g.152470609T>C , CM000668.1:g.152470609T>C | GRCh37 |
| NC_000006.10:g.152512302T>C | NCBI36 |
| NG_012855.1:g.492926A>G | |
| NG_012855.2:g.492926A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354674.5:c.1107+3A>G MANE Plus Clinical | ENSP00000346701.4:n.1107+3A>G | |
| ENST00000367255.10:c.24642+3A>G MANE Select | ENSP00000356224.5:n.24642+3A>G | |
| ENST00000423061.6:c.24429+3A>G | ENSP00000396024.1:n.24429+3A>G | |
| ENST00000672154.1:c.158+3A>G | ||
| ENST00000672169.1:c.377+3A>G | ||
| ENST00000673173.1:c.556+3A>G | ||
| ENST00000673451.1:c.414+3A>G | ENSP00000500189.1:n.414+3A>G | |
| ENST00000341594.9:c.23427+3A>G | ENSP00000341887.6:n.23427+3A>G | |
| ENST00000347037.9:n.1321+3A>G | ||
| ENST00000354674.4:c.1107+3A>G | ENSP00000346701.4:n.1107+3A>G | |
| ENST00000367251.7:c.3408+3A>G | ENSP00000356220.3:n.3408+3A>G | |
| ENST00000367255.9:c.24642+3A>G | ENSP00000356224.5:n.24642+3A>G | |
| ENST00000367256.9:n.8334+3A>G | ||
| ENST00000367257.8:c.2580+3A>G | ENSP00000356226.4:n.2580+3A>G | |
| ENST00000409694.6:n.8226+3A>G | ||
| ENST00000423061.5:c.24429+3A>G | ENSP00000396024.1:n.24429+3A>G | |
| ENST00000460912.6:n.1187+3A>G | ||
| ENST00000472563.2:n.30+3A>G | ||
| ENST00000536990.5:n.1479+3A>G | ||
| ENST00000539504.5:c.1107+3A>G | ENSP00000441052.1:n.1107+3A>G | |
| NM_033071.3:c.24429+3A>G | NP_149062.1:n.24429+3A>G | |
| NM_182961.3:c.24642+3A>G | NP_892006.3:n.24642+3A>G | |
| XM_006715407.1:c.24678+3A>G | XP_006715470.1:n.24678+3A>G | |
| XM_006715408.1:c.24666+3A>G | XP_006715471.1:n.24666+3A>G | |
| XM_006715409.1:c.24657+3A>G | XP_006715472.1:n.24657+3A>G | |
| XM_006715410.1:c.24678+3A>G | XP_006715473.1:n.24678+3A>G | |
| XM_006715411.1:c.24627+3A>G | XP_006715474.1:n.24627+3A>G | |
| XM_006715412.1:c.24663+3A>G | XP_006715475.1:n.24663+3A>G | |
| XM_006715413.1:c.24678+3A>G | XP_006715476.1:n.24678+3A>G | |
| XM_006715414.1:c.24606+3A>G | XP_006715477.1:n.24606+3A>G | |
| XM_006715415.1:c.24678+3A>G | XP_006715478.1:n.24678+3A>G | |
| XM_006715416.1:c.24663+3A>G | XP_006715479.1:n.24663+3A>G | |
| XM_006715417.1:c.24537+3A>G | XP_006715480.1:n.24537+3A>G | |
| XM_006715420.1:c.24525+3A>G | XP_006715483.1:n.24525+3A>G | |
| XM_006715421.1:c.24522+3A>G | XP_006715484.1:n.24522+3A>G | |
| XM_006715422.1:c.24519+3A>G | XP_006715485.1:n.24519+3A>G | |
| XM_006715423.1:c.24678+3A>G | XP_006715486.1:n.24678+3A>G | |
| XM_006715424.1:c.24678+3A>G | XP_006715487.1:n.24678+3A>G | |
| XM_006715425.1:c.24678+3A>G | XP_006715488.1:n.24678+3A>G | |
| XM_011535641.1:c.24675+3A>G | XP_011533943.1:n.24675+3A>G | |
| XM_011535642.1:c.24663+3A>G | XP_011533944.1:n.24663+3A>G | |
| XM_011535643.1:c.24513+3A>G | XP_011533945.1:n.24513+3A>G | |
| XM_011535644.1:c.22953+3A>G | XP_011533946.1:n.22953+3A>G | |
| XM_011535645.1:c.22446+3A>G | XP_011533947.1:n.22446+3A>G | |
| XM_011535647.1:c.17913+3A>G | XP_011533949.1:n.17913+3A>G | |
| NM_001347701.1:c.1248+3A>G | NP_001334630.1:n.1248+3A>G | |
| NM_001347702.1:c.1107+3A>G | NP_001334631.1:n.1107+3A>G | |
| XM_006715408.2:c.24666+3A>G | XP_006715471.1:n.24666+3A>G | |
| XM_006715410.2:c.24678+3A>G | XP_006715473.1:n.24678+3A>G | |
| XM_006715412.2:c.24663+3A>G | XP_006715475.1:n.24663+3A>G | |
| XM_006715413.2:c.24678+3A>G | XP_006715476.1:n.24678+3A>G | |
| XM_006715415.2:c.24678+3A>G | XP_006715478.1:n.24678+3A>G | |
| XM_006715416.2:c.24663+3A>G | XP_006715479.1:n.24663+3A>G | |
| XM_006715417.2:c.24537+3A>G | XP_006715480.1:n.24537+3A>G | |
| XM_006715420.2:c.24525+3A>G | XP_006715483.1:n.24525+3A>G | |
| XM_006715421.2:c.24522+3A>G | XP_006715484.1:n.24522+3A>G | |
| XM_006715423.2:c.24678+3A>G | XP_006715486.1:n.24678+3A>G | |
| XM_006715424.2:c.24678+3A>G | XP_006715487.1:n.24678+3A>G | |
| XM_006715425.2:c.24678+3A>G | XP_006715488.1:n.24678+3A>G | |
| XM_011535641.2:c.24675+3A>G | XP_011533943.1:n.24675+3A>G | |
| XM_011535642.2:c.24663+3A>G | XP_011533944.1:n.24663+3A>G | |
| XM_011535645.2:c.22446+3A>G | XP_011533947.1:n.22446+3A>G | |
| XM_017010608.1:c.24678+3A>G | XP_016866097.1:n.24678+3A>G | |
| XM_017010609.1:c.24678+3A>G | XP_016866098.1:n.24678+3A>G | |
| XM_017010610.1:c.24657+3A>G | XP_016866099.1:n.24657+3A>G | |
| XM_017010611.2:c.24651+3A>G | XP_016866100.1:n.24651+3A>G | |
| XM_017010612.1:c.24600+3A>G | XP_016866101.1:n.24600+3A>G | |
| XM_017010613.1:c.24675+3A>G | XP_016866102.1:n.24675+3A>G | |
| XM_017010614.1:c.24522+3A>G | XP_016866103.1:n.24522+3A>G | |
| XM_017010615.1:c.24522+3A>G | XP_016866104.1:n.24522+3A>G | |
| XM_017010616.1:c.24678+3A>G | XP_016866105.1:n.24678+3A>G | |
| XM_017010617.1:c.24675+3A>G | XP_016866106.1:n.24675+3A>G | |
| XM_017010618.1:c.24663+3A>G | XP_016866107.1:n.24663+3A>G | |
| XM_017010619.1:c.22953+3A>G | XP_016866108.1:n.22953+3A>G | |
| NM_182961.4:c.24642+3A>G MANE Select | NP_892006.3:n.24642+3A>G | |
| NM_001347701.2:c.1248+3A>G | NP_001334630.1:n.1248+3A>G | |
| NM_001347702.2:c.1107+3A>G MANE Plus Clinical | NP_001334631.1:n.1107+3A>G | |
| NM_033071.5:c.24429+3A>G | NP_149062.2:n.24429+3A>G |