Linked Data
ClinVar Variation Id:
445622
dbSNP Id:
rs371223664
ExAC:
12:49428255 C / T
gnomAD v2:
12-49428255-C-T
gnomAD v3:
12-49034472-C-T
gnomAD v4:
12-49034472-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.49034472C>T , CM000674.2:g.49034472C>T | GRCh38 |
| NC_000012.11:g.49428255C>T , CM000674.1:g.49428255C>T | GRCh37 |
| NC_000012.10:g.47714522C>T | NCBI36 |
| NG_027827.1:g.25853G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683543.2:c.10445G>A | ENSP00000506726.1:p.Arg3482Gln | |
| ENST00000685166.1:c.10454G>A | ENSP00000509386.1:p.Arg3485Gln | |
| ENST00000685554.1:c.5G>A | ENSP00000508640.1:p.Arg2Gln | |
| ENST00000687201.1:c.2024G>A | ENSP00000510037.1:p.Arg675Gln | |
| ENST00000692637.1:c.10442G>A | ENSP00000509666.1:p.Arg3481Gln | |
| ENST00000692841.1:c.1924G>A | ENSP00000508711.1:p.Gly642Arg | |
| ENST00000301067.12:c.10445G>A MANE Select | ENSP00000301067.7:p.Arg3482Gln | |
| ENST00000301067.11:c.10445G>A | ENSP00000301067.7:p.Arg3482Gln | |
| NM_003482.3:c.10445G>A | NP_003473.3:p.Arg3482Gln | |
| XM_005269162.3:c.10445G>A | XP_005269219.1:p.Arg3482Gln | |
| XM_006719614.2:c.10454G>A | XP_006719677.1:p.Arg3485Gln | |
| XM_006719616.2:c.10442G>A | XP_006719679.1:p.Arg3481Gln | |
| XM_011538770.1:c.10454G>A | XP_011537072.1:p.Arg3485Gln | |
| XM_011538771.1:c.10451G>A | XP_011537073.1:p.Arg3484Gln | |
| XM_011538772.1:c.10445G>A | XP_011537074.1:p.Arg3482Gln | |
| XM_011538773.1:c.10442G>A | XP_011537075.1:p.Arg3481Gln | |
| XM_011538774.1:c.10433G>A | XP_011537076.1:p.Arg3478Gln | |
| XM_011538775.1:c.10454G>A | XP_011537077.1:p.Arg3485Gln | |
| XM_011538776.1:c.10361G>A | XP_011537078.1:p.Arg3454Gln | |
| XR_944740.1:n.12774G>A | ||
| XM_005269162.4:c.10445G>A | XP_005269219.1:p.Arg3482Gln | |
| XM_006719614.4:c.10454G>A | XP_006719677.1:p.Arg3485Gln | |
| XM_006719616.3:c.10442G>A | XP_006719679.1:p.Arg3481Gln | |
| XM_011538770.2:c.10454G>A | XP_011537072.1:p.Arg3485Gln | |
| XM_011538771.2:c.10451G>A | XP_011537073.1:p.Arg3484Gln | |
| XM_011538772.2:c.10445G>A | XP_011537074.1:p.Arg3482Gln | |
| XM_011538773.2:c.10442G>A | XP_011537075.1:p.Arg3481Gln | |
| XM_011538774.2:c.10433G>A | XP_011537076.1:p.Arg3478Gln | |
| XM_011538776.2:c.10361G>A | XP_011537078.1:p.Arg3454Gln | |
| XR_001748874.1:n.11763G>A | ||
| NM_003482.4:c.10445G>A MANE Select | NP_003473.3:p.Arg3482Gln |