Linked Data
ClinVar Variation Id:
235346
dbSNP Id:
rs182849552
ExAC:
15:55497811 C / T
gnomAD v2:
15-55497811-C-T
gnomAD v3:
15-55205613-C-T
gnomAD v4:
15-55205613-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.55205613C>T , CM000677.2:g.55205613C>T | GRCh38 |
| NC_000015.9:g.55497811C>T , CM000677.1:g.55497811C>T | GRCh37 |
| NC_000015.8:g.53285103C>T | NCBI36 |
| NG_009103.1:g.89191G>A , LRG_96:g.89191G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000697641.1:n.2596G>A | ||
| ENST00000697642.1:c.560G>A | ENSP00000513368.1:p.Arg187Gln | |
| ENST00000697643.1:c.560G>A | ENSP00000513369.1:p.Arg187Gln | |
| ENST00000697644.1:n.2728G>A | ||
| ENST00000336787.6:c.560G>A MANE Select | ENSP00000337761.1:p.Arg187Gln | |
| ENST00000336787.5:c.560G>A | ENSP00000337761.1:p.Arg187Gln | |
| ENST00000396307.6:c.560G>A | ENSP00000379601.2:p.Arg187Gln | |
| ENST00000564609.5:c.560G>A | ENSP00000455012.1:p.Arg187Gln | |
| ENST00000569493.5:c.560G>A | ENSP00000456059.1:p.Arg187Gln | |
| NM_004580.4:c.560G>A | NP_004571.2:p.Arg187Gln | |
| NM_183234.2:c.560G>A | NP_899057.1:p.Arg187Gln | |
| NM_183235.2:c.560G>A | NP_899058.1:p.Arg187Gln | |
| NM_183236.2:c.560G>A | NP_899059.1:p.Arg187Gln | |
| XM_005254576.3:c.560G>A | XP_005254633.1:p.Arg187Gln | |
| XM_011521852.1:c.560G>A | XP_011520154.1:p.Arg187Gln | |
| XM_011521853.1:c.560G>A | XP_011520155.1:p.Arg187Gln | |
| XM_011521854.1:c.560G>A | XP_011520156.1:p.Arg187Gln | |
| XM_011521855.1:c.560G>A | XP_011520157.1:p.Arg187Gln | |
| XM_011521856.1:c.560G>A | XP_011520158.1:p.Arg187Gln | |
| XM_005254576.5:c.560G>A | XP_005254633.1:p.Arg187Gln | |
| XM_011521855.3:c.560G>A | XP_011520157.1:p.Arg187Gln | |
| XM_011521856.2:c.560G>A | XP_011520158.1:p.Arg187Gln | |
| XM_024450009.1:c.560G>A | XP_024305777.1:p.Arg187Gln | |
| NM_183235.3:c.560G>A MANE Select | NP_899058.1:p.Arg187Gln | |
| NM_004580.5:c.560G>A | NP_004571.2:p.Arg187Gln | |
| NM_183236.3:c.560G>A | NP_899059.1:p.Arg187Gln |