Linked Data
ClinVar Variation Id:
229421
ClinVar RCV Id:
RCV000213570
RCV000529922
RCV000733721
RCV001130797
RCV001130798
RCV001130799
RCV001133756
RCV001133757
dbSNP Id:
rs368777046
ExAC:
2:179545841 C / T
gnomAD v2:
2-179545841-C-T
gnomAD v3:
2-178681114-C-T
gnomAD v4:
2-178681114-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178681114C>T , CM000664.2:g.178681114C>T | GRCh38 |
| NC_000002.11:g.179545841C>T , CM000664.1:g.179545841C>T | GRCh37 |
| NC_000002.10:g.179254086C>T | NCBI36 |
| NG_011618.3:g.154689G>A , LRG_391:g.154689G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.29573G>A | ENSP00000343764.6:p.Arg9858His | |
| ENST00000342175.11:c.13859-38797G>A | ENSP00000340554.6:n.13859-38797G>A | |
| ENST00000359218.10:c.13658-38797G>A | ENSP00000352154.5:n.13658-38797G>A | |
| ENST00000342175.10:c.13859-38797G>A | ENSP00000340554.6:n.13859-38797G>A | |
| ENST00000342992.10:c.29573G>A | ENSP00000343764.6:p.Arg9858His | |
| ENST00000359218.9:c.13658-38797G>A | ENSP00000352154.5:n.13658-38797G>A | |
| ENST00000414766.5:c.2014+547G>A | ENSP00000401501.1:n.2014+547G>A | |
| ENST00000460472.6:c.13283-38797G>A | ENSP00000434586.1:n.13283-38797G>A | |
| ENST00000589042.5:c.33305G>A MANE Select | ENSP00000467141.1:p.Arg11102His | |
| ENST00000591111.5:c.32354G>A | ENSP00000465570.1:p.Arg10785His | |
| ENST00000615779.4:c.32354G>A | ENSP00000483597.1:p.Arg10785His | |
| NM_001256850.1:c.32354G>A | NP_001243779.1:p.Arg10785His | |
| NM_001267550.2:c.33305G>A MANE Select | NP_001254479.2:p.Arg11102His | |
| NM_003319.4:c.13283-38797G>A | NP_003310.4:n.13283-38797G>A | |
| NM_133378.4:c.29573G>A | NP_596869.4:p.Arg9858His | |
| NM_133432.3:c.13658-38797G>A | NP_597676.3:n.13658-38797G>A | |
| NM_133437.4:c.13859-38797G>A | NP_597681.4:n.13859-38797G>A | |
| XM_011511729.1:c.32402G>A | XP_011510031.1:p.Arg10801His | |
| XM_011511730.1:c.13469-38797G>A | XP_011510032.1:n.13469-38797G>A | |
| XM_011511731.1:c.13328-38797G>A | XP_011510033.1:n.13328-38797G>A | |
| XM_017004819.1:c.32357G>A | XP_016860308.1:p.Arg10786His | |
| XM_017004820.1:c.29576G>A | XP_016860309.1:p.Arg9859His | |
| XM_017004821.1:c.29573G>A | XP_016860310.1:p.Arg9858His | |
| XM_017004822.1:c.31432+547G>A | XP_016860311.1:n.31432+547G>A | |
| XM_017004823.1:c.13424-38797G>A | XP_016860312.1:n.13424-38797G>A | |
| XM_024453094.1:c.32357G>A | XP_024308862.1:p.Arg10786His | |
| XM_024453095.1:c.32357G>A | XP_024308863.1:p.Arg10786His | |
| XM_024453096.1:c.32224+547G>A | XP_024308864.1:n.32224+547G>A | |
| XM_024453097.1:c.31264+547G>A | XP_024308865.1:n.31264+547G>A | |
| XM_024453098.1:c.31183+547G>A | XP_024308866.1:n.31183+547G>A | |
| XM_024453099.1:c.13424-38797G>A | XP_024308867.1:n.13424-38797G>A |