Linked Data
ClinVar Variation Id:
290009
dbSNP Id:
rs563400584
ExAC:
6:152650857 A / G
gnomAD v2:
6-152650857-A-G
gnomAD v3:
6-152329722-A-G
gnomAD v4:
6-152329722-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152329722A>G , CM000668.2:g.152329722A>G | GRCh38 |
| NC_000006.11:g.152650857A>G , CM000668.1:g.152650857A>G | GRCh37 |
| NC_000006.10:g.152692550A>G | NCBI36 |
| NG_012855.1:g.312678T>C | |
| NG_012855.2:g.312678T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367255.10:c.14955+8T>C MANE Select | ENSP00000356224.5:n.14955+8T>C | |
| ENST00000423061.6:c.14742+8T>C | ENSP00000396024.1:n.14742+8T>C | |
| ENST00000341594.9:c.14145+8T>C | ENSP00000341887.6:n.14145+8T>C | |
| ENST00000367255.9:c.14955+8T>C | ENSP00000356224.5:n.14955+8T>C | |
| ENST00000423061.5:c.14742+8T>C | ENSP00000396024.1:n.14742+8T>C | |
| ENST00000448038.2:c.-964+8T>C | ENSP00000390975.2:n.-964+8T>C | |
| ENST00000490135.6:n.2301+8T>C | ||
| NM_033071.3:c.14742+8T>C | NP_149062.1:n.14742+8T>C | |
| NM_182961.3:c.14955+8T>C | NP_892006.3:n.14955+8T>C | |
| XM_006715407.1:c.14976+8T>C | XP_006715470.1:n.14976+8T>C | |
| XM_006715408.1:c.14976+8T>C | XP_006715471.1:n.14976+8T>C | |
| XM_006715409.1:c.14955+8T>C | XP_006715472.1:n.14955+8T>C | |
| XM_006715410.1:c.14976+8T>C | XP_006715473.1:n.14976+8T>C | |
| XM_006715411.1:c.14925+8T>C | XP_006715474.1:n.14925+8T>C | |
| XM_006715412.1:c.14976+8T>C | XP_006715475.1:n.14976+8T>C | |
| XM_006715413.1:c.14976+8T>C | XP_006715476.1:n.14976+8T>C | |
| XM_006715414.1:c.14904+8T>C | XP_006715477.1:n.14904+8T>C | |
| XM_006715415.1:c.14976+8T>C | XP_006715478.1:n.14976+8T>C | |
| XM_006715416.1:c.14976+8T>C | XP_006715479.1:n.14976+8T>C | |
| XM_006715417.1:c.14976+8T>C | XP_006715480.1:n.14976+8T>C | |
| XM_006715420.1:c.14976+8T>C | XP_006715483.1:n.14976+8T>C | |
| XM_006715421.1:c.14820+8T>C | XP_006715484.1:n.14820+8T>C | |
| XM_006715422.1:c.14817+8T>C | XP_006715485.1:n.14817+8T>C | |
| XM_006715423.1:c.14976+8T>C | XP_006715486.1:n.14976+8T>C | |
| XM_006715424.1:c.14976+8T>C | XP_006715487.1:n.14976+8T>C | |
| XM_006715425.1:c.14976+8T>C | XP_006715488.1:n.14976+8T>C | |
| XM_011535641.1:c.14976+8T>C | XP_011533943.1:n.14976+8T>C | |
| XM_011535642.1:c.14976+8T>C | XP_011533944.1:n.14976+8T>C | |
| XM_011535643.1:c.14811+8T>C | XP_011533945.1:n.14811+8T>C | |
| XM_011535644.1:c.13251+8T>C | XP_011533946.1:n.13251+8T>C | |
| XM_011535645.1:c.12744+8T>C | XP_011533947.1:n.12744+8T>C | |
| XM_011535646.1:c.14976+8T>C | XP_011533948.1:n.14976+8T>C | |
| XM_011535647.1:c.8211+8T>C | XP_011533949.1:n.8211+8T>C | |
| XM_006715408.2:c.14976+8T>C | XP_006715471.1:n.14976+8T>C | |
| XM_006715410.2:c.14976+8T>C | XP_006715473.1:n.14976+8T>C | |
| XM_006715412.2:c.14976+8T>C | XP_006715475.1:n.14976+8T>C | |
| XM_006715413.2:c.14976+8T>C | XP_006715476.1:n.14976+8T>C | |
| XM_006715415.2:c.14976+8T>C | XP_006715478.1:n.14976+8T>C | |
| XM_006715416.2:c.14976+8T>C | XP_006715479.1:n.14976+8T>C | |
| XM_006715417.2:c.14976+8T>C | XP_006715480.1:n.14976+8T>C | |
| XM_006715420.2:c.14976+8T>C | XP_006715483.1:n.14976+8T>C | |
| XM_006715421.2:c.14820+8T>C | XP_006715484.1:n.14820+8T>C | |
| XM_006715423.2:c.14976+8T>C | XP_006715486.1:n.14976+8T>C | |
| XM_006715424.2:c.14976+8T>C | XP_006715487.1:n.14976+8T>C | |
| XM_006715425.2:c.14976+8T>C | XP_006715488.1:n.14976+8T>C | |
| XM_011535641.2:c.14976+8T>C | XP_011533943.1:n.14976+8T>C | |
| XM_011535642.2:c.14976+8T>C | XP_011533944.1:n.14976+8T>C | |
| XM_011535645.2:c.12744+8T>C | XP_011533947.1:n.12744+8T>C | |
| XM_017010608.1:c.14976+8T>C | XP_016866097.1:n.14976+8T>C | |
| XM_017010609.1:c.14976+8T>C | XP_016866098.1:n.14976+8T>C | |
| XM_017010610.1:c.14955+8T>C | XP_016866099.1:n.14955+8T>C | |
| XM_017010611.2:c.14949+8T>C | XP_016866100.1:n.14949+8T>C | |
| XM_017010612.1:c.14898+8T>C | XP_016866101.1:n.14898+8T>C | |
| XM_017010613.1:c.14976+8T>C | XP_016866102.1:n.14976+8T>C | |
| XM_017010614.1:c.14976+8T>C | XP_016866103.1:n.14976+8T>C | |
| XM_017010615.1:c.14976+8T>C | XP_016866104.1:n.14976+8T>C | |
| XM_017010616.1:c.14976+8T>C | XP_016866105.1:n.14976+8T>C | |
| XM_017010617.1:c.14976+8T>C | XP_016866106.1:n.14976+8T>C | |
| XM_017010618.1:c.14976+8T>C | XP_016866107.1:n.14976+8T>C | |
| XM_017010619.1:c.13251+8T>C | XP_016866108.1:n.13251+8T>C | |
| XR_001743287.1:n.15459+8T>C | ||
| NM_182961.4:c.14955+8T>C MANE Select | NP_892006.3:n.14955+8T>C | |
| NM_033071.5:c.14742+8T>C | NP_149062.2:n.14742+8T>C |