Linked Data
ClinVar Variation Id:
166076
dbSNP Id:
rs571348685
ExAC:
2:179507020 C / T
gnomAD v2:
2-179507020-C-T
gnomAD v3:
2-178642293-C-T
gnomAD v4:
2-178642293-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178642293C>T , CM000664.2:g.178642293C>T | GRCh38 |
| NC_000002.11:g.179507020C>T , CM000664.1:g.179507020C>T | GRCh37 |
| NC_000002.10:g.179215265C>T | NCBI36 |
| NG_011618.3:g.193510G>A , LRG_391:g.193510G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.32798G>A | ENSP00000343764.6:p.Arg10933His | |
| ENST00000342175.11:c.13883G>A | ENSP00000340554.6:p.Arg4628His | |
| ENST00000359218.10:c.13682G>A | ENSP00000352154.5:p.Arg4561His | |
| ENST00000342175.10:c.13883G>A | ENSP00000340554.6:p.Arg4628His | |
| ENST00000342992.10:c.32798G>A | ENSP00000343764.6:p.Arg10933His | |
| ENST00000359218.9:c.13682G>A | ENSP00000352154.5:p.Arg4561His | |
| ENST00000414766.5:c.2465G>A | ENSP00000401501.1:p.Arg822His | |
| ENST00000426232.5:c.597-1663G>A | ||
| ENST00000446966.1:c.995-1663G>A | ENSP00000408004.1:n.995-1663G>A | |
| ENST00000460472.6:c.13307G>A | ENSP00000434586.1:p.Arg4436His | |
| ENST00000589042.5:c.40502G>A MANE Select | ENSP00000467141.1:p.Arg13501His | |
| ENST00000591111.5:c.35579G>A | ENSP00000465570.1:p.Arg11860His | |
| ENST00000615779.4:c.35579G>A | ENSP00000483597.1:p.Arg11860His | |
| NM_001256850.1:c.35579G>A | NP_001243779.1:p.Arg11860His | |
| NM_001267550.2:c.40502G>A MANE Select | NP_001254479.2:p.Arg13501His | |
| NM_003319.4:c.13307G>A | NP_003310.4:p.Arg4436His | |
| NM_133378.4:c.32798G>A | NP_596869.4:p.Arg10933His | |
| NM_133432.3:c.13682G>A | NP_597676.3:p.Arg4561His | |
| NM_133437.4:c.13883G>A | NP_597681.4:p.Arg4628His | |
| XM_011511729.1:c.39599G>A | XP_011510031.1:p.Arg13200His | |
| XM_011511730.1:c.13493G>A | XP_011510032.1:p.Arg4498His | |
| XM_011511731.1:c.13352G>A | XP_011510033.1:p.Arg4451His | |
| XM_017004819.1:c.39395G>A | XP_016860308.1:p.Arg13132His | |
| XM_017004820.1:c.34793G>A | XP_016860309.1:p.Arg11598His | |
| XM_017004821.1:c.34790G>A | XP_016860310.1:p.Arg11597His | |
| XM_017004822.1:c.31883G>A | XP_016860311.1:p.Arg10628His | |
| XM_017004823.1:c.13448G>A | XP_016860312.1:p.Arg4483His | |
| XM_024453094.1:c.34943G>A | XP_024308862.1:p.Arg11648His | |
| XM_024453095.1:c.34940G>A | XP_024308863.1:p.Arg11647His | |
| XM_024453096.1:c.34373G>A | XP_024308864.1:p.Arg11458His | |
| XM_024453097.1:c.31715G>A | XP_024308865.1:p.Arg10572His | |
| XM_024453098.1:c.31634G>A | XP_024308866.1:p.Arg10545His | |
| XM_024453099.1:c.13448G>A | XP_024308867.1:p.Arg4483His | |
| XM_024453100.1:c.3251G>A | XP_024308868.1:p.Arg1084His |