Linked Data
ClinVar Variation Id:
465779
dbSNP Id:
rs759460806
ExAC:
6:152639400 T / G
gnomAD v2:
6-152639400-T-G
gnomAD v3:
6-152318265-T-G
gnomAD v4:
6-152318265-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152318265T>G , CM000668.2:g.152318265T>G | GRCh38 |
| NC_000006.11:g.152639400T>G , CM000668.1:g.152639400T>G | GRCh37 |
| NC_000006.10:g.152681093T>G | NCBI36 |
| NG_012855.1:g.324135A>C | |
| NG_012855.2:g.324135A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000448038.3:n.868-2A>C | ||
| ENST00000682179.1:n.461-2A>C | ||
| ENST00000682252.1:n.461-2A>C | ||
| ENST00000684208.1:n.461-2A>C | ||
| ENST00000684643.1:n.550-2A>C | ||
| ENST00000367255.10:c.16390-2A>C MANE Select | ENSP00000356224.5:n.16390-2A>C | |
| ENST00000423061.6:c.16177-2A>C | ENSP00000396024.1:n.16177-2A>C | |
| ENST00000341594.9:c.15357+598A>C | ENSP00000341887.6:n.15357+598A>C | |
| ENST00000367255.9:c.16390-2A>C | ENSP00000356224.5:n.16390-2A>C | |
| ENST00000367256.9:n.80A>C | ||
| ENST00000423061.5:c.16177-2A>C | ENSP00000396024.1:n.16177-2A>C | |
| ENST00000448038.2:c.790-2A>C | ENSP00000390975.2:n.790-2A>C | |
| ENST00000490135.6:n.3736-2A>C | ||
| NM_033071.3:c.16177-2A>C | NP_149062.1:n.16177-2A>C | |
| NM_182961.3:c.16390-2A>C | NP_892006.3:n.16390-2A>C | |
| XM_006715407.1:c.16411-2A>C | XP_006715470.1:n.16411-2A>C | |
| XM_006715408.1:c.16411-2A>C | XP_006715471.1:n.16411-2A>C | |
| XM_006715409.1:c.16390-2A>C | XP_006715472.1:n.16390-2A>C | |
| XM_006715410.1:c.16411-2A>C | XP_006715473.1:n.16411-2A>C | |
| XM_006715411.1:c.16360-2A>C | XP_006715474.1:n.16360-2A>C | |
| XM_006715412.1:c.16411-2A>C | XP_006715475.1:n.16411-2A>C | |
| XM_006715413.1:c.16411-2A>C | XP_006715476.1:n.16411-2A>C | |
| XM_006715414.1:c.16339-2A>C | XP_006715477.1:n.16339-2A>C | |
| XM_006715415.1:c.16411-2A>C | XP_006715478.1:n.16411-2A>C | |
| XM_006715416.1:c.16411-2A>C | XP_006715479.1:n.16411-2A>C | |
| XM_006715417.1:c.16411-2A>C | XP_006715480.1:n.16411-2A>C | |
| XM_006715420.1:c.16411-2A>C | XP_006715483.1:n.16411-2A>C | |
| XM_006715421.1:c.16255-2A>C | XP_006715484.1:n.16255-2A>C | |
| XM_006715422.1:c.16252-2A>C | XP_006715485.1:n.16252-2A>C | |
| XM_006715423.1:c.16411-2A>C | XP_006715486.1:n.16411-2A>C | |
| XM_006715424.1:c.16411-2A>C | XP_006715487.1:n.16411-2A>C | |
| XM_006715425.1:c.16411-2A>C | XP_006715488.1:n.16411-2A>C | |
| XM_011535641.1:c.16411-2A>C | XP_011533943.1:n.16411-2A>C | |
| XM_011535642.1:c.16411-2A>C | XP_011533944.1:n.16411-2A>C | |
| XM_011535643.1:c.16246-2A>C | XP_011533945.1:n.16246-2A>C | |
| XM_011535644.1:c.14686-2A>C | XP_011533946.1:n.14686-2A>C | |
| XM_011535645.1:c.14179-2A>C | XP_011533947.1:n.14179-2A>C | |
| XM_011535646.1:c.16411-2A>C | XP_011533948.1:n.16411-2A>C | |
| XM_011535647.1:c.9646-2A>C | XP_011533949.1:n.9646-2A>C | |
| XM_006715408.2:c.16411-2A>C | XP_006715471.1:n.16411-2A>C | |
| XM_006715410.2:c.16411-2A>C | XP_006715473.1:n.16411-2A>C | |
| XM_006715412.2:c.16411-2A>C | XP_006715475.1:n.16411-2A>C | |
| XM_006715413.2:c.16411-2A>C | XP_006715476.1:n.16411-2A>C | |
| XM_006715415.2:c.16411-2A>C | XP_006715478.1:n.16411-2A>C | |
| XM_006715416.2:c.16411-2A>C | XP_006715479.1:n.16411-2A>C | |
| XM_006715417.2:c.16411-2A>C | XP_006715480.1:n.16411-2A>C | |
| XM_006715420.2:c.16411-2A>C | XP_006715483.1:n.16411-2A>C | |
| XM_006715421.2:c.16255-2A>C | XP_006715484.1:n.16255-2A>C | |
| XM_006715423.2:c.16411-2A>C | XP_006715486.1:n.16411-2A>C | |
| XM_006715424.2:c.16411-2A>C | XP_006715487.1:n.16411-2A>C | |
| XM_006715425.2:c.16411-2A>C | XP_006715488.1:n.16411-2A>C | |
| XM_011535641.2:c.16411-2A>C | XP_011533943.1:n.16411-2A>C | |
| XM_011535642.2:c.16411-2A>C | XP_011533944.1:n.16411-2A>C | |
| XM_011535645.2:c.14179-2A>C | XP_011533947.1:n.14179-2A>C | |
| XM_017010608.1:c.16411-2A>C | XP_016866097.1:n.16411-2A>C | |
| XM_017010609.1:c.16411-2A>C | XP_016866098.1:n.16411-2A>C | |
| XM_017010610.1:c.16390-2A>C | XP_016866099.1:n.16390-2A>C | |
| XM_017010611.2:c.16384-2A>C | XP_016866100.1:n.16384-2A>C | |
| XM_017010612.1:c.16333-2A>C | XP_016866101.1:n.16333-2A>C | |
| XM_017010613.1:c.16411-2A>C | XP_016866102.1:n.16411-2A>C | |
| XM_017010614.1:c.16411-2A>C | XP_016866103.1:n.16411-2A>C | |
| XM_017010615.1:c.16411-2A>C | XP_016866104.1:n.16411-2A>C | |
| XM_017010616.1:c.16411-2A>C | XP_016866105.1:n.16411-2A>C | |
| XM_017010617.1:c.16411-2A>C | XP_016866106.1:n.16411-2A>C | |
| XM_017010618.1:c.16411-2A>C | XP_016866107.1:n.16411-2A>C | |
| XM_017010619.1:c.14686-2A>C | XP_016866108.1:n.14686-2A>C | |
| XR_001743287.1:n.16894-2A>C | ||
| NM_182961.4:c.16390-2A>C MANE Select | NP_892006.3:n.16390-2A>C | |
| NM_033071.5:c.16177-2A>C | NP_149062.2:n.16177-2A>C |