Linked Data
ClinVar Variation Id:
502601
dbSNP Id:
rs782269360
ExAC:
1:120491183 C / T
gnomAD v2:
1-120491183-C-T
gnomAD v3:
1-119948560-C-T
gnomAD v4:
1-119948560-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119948560C>T , CM000663.2:g.119948560C>T | GRCh38 |
| NC_000001.10:g.120491183C>T , CM000663.1:g.120491183C>T | GRCh37 |
| NC_000001.9:g.120292706C>T | NCBI36 |
| NG_008163.1:g.126094G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256646.7:c.2606G>A MANE Select | ENSP00000256646.2:p.Arg869Gln | |
| ENST00000256646.6:c.2606G>A | ENSP00000256646.2:p.Arg869Gln | |
| NM_001200001.1:c.2606G>A | NP_001186930.1:p.Arg869Gln | |
| NM_024408.3:c.2606G>A | NP_077719.2:p.Arg869Gln | |
| XM_005270901.2:c.2489G>A | XP_005270958.1:p.Arg830Gln | |
| XM_011541519.1:c.2594G>A | XP_011539821.1:p.Arg865Gln | |
| XM_011541520.1:c.2489G>A | XP_011539822.1:p.Arg830Gln | |
| NM_024408.4:c.2606G>A MANE Select | NP_077719.2:p.Arg869Gln | |
| NM_001200001.2:c.2606G>A | NP_001186930.1:p.Arg869Gln |