Linked Data
ClinVar Variation Id:
876509
dbSNP Id:
rs61755431
ExAC:
1:155260382 C / T
gnomAD v2:
1-155260382-C-T
gnomAD v3:
1-155290591-C-T
gnomAD v4:
1-155290591-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.155290591C>T , CM000663.2:g.155290591C>T | GRCh38 |
| NC_000001.10:g.155260382C>T , CM000663.1:g.155260382C>T | GRCh37 |
| NC_000001.9:g.153527006C>T | NCBI36 |
| NG_011677.1:g.15844G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342741.6:c.1706G>A MANE Select | ENSP00000339933.4:p.Arg569Gln | |
| ENST00000342741.4:c.1706G>A | ENSP00000339933.4:p.Arg569Gln | |
| ENST00000392414.7:c.1613G>A | ENSP00000376214.3:p.Arg538Gln | |
| NM_000298.5:c.1706G>A | NP_000289.1:p.Arg569Gln | |
| NM_181871.3:c.1613G>A | NP_870986.1:p.Arg538Gln | |
| XM_005245266.3:c.1865G>A | XP_005245323.1:p.Arg622Gln | |
| XM_006711386.2:c.1514G>A | XP_006711449.1:p.Arg505Gln | |
| XM_011509640.1:c.1514G>A | XP_011507942.1:p.Arg505Gln | |
| NM_000298.6:c.1706G>A MANE Select | NP_000289.1:p.Arg569Gln | |
| XM_006711386.4:c.1514G>A | XP_006711449.1:p.Arg505Gln | |
| XM_011509640.3:c.1514G>A | XP_011507942.1:p.Arg505Gln | |
| NM_181871.4:c.1613G>A | NP_870986.1:p.Arg538Gln |