Linked Data
ClinVar Variation Id:
206587
dbSNP Id:
rs796052902
gnomAD v2:
15-89872334-C-T
gnomAD v3:
15-89329103-C-T
gnomAD v4:
15-89329103-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89329103C>T , CM000677.2:g.89329103C>T | GRCh38 |
| NC_000015.9:g.89872334C>T , CM000677.1:g.89872334C>T | GRCh37 |
| NC_000015.8:g.87673338C>T | NCBI36 |
| NG_008218.1:g.10693G>A | |
| NG_008218.2:g.10693G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000636937.2:c.863G>A | ENSP00000516154.1:p.Arg288His | |
| ENST00000268124.11:c.863G>A MANE Select | ENSP00000268124.5:p.Arg288His | |
| ENST00000530292.3:c.464G>A | ENSP00000432885.2:p.Arg155His | |
| ENST00000635986.2:c.863G>A | ENSP00000490653.2:p.Arg288His | |
| ENST00000636774.1:c.863G>A | ENSP00000489799.1:p.Arg288His | |
| ENST00000666746.1:c.520G>A | ||
| ENST00000672071.1:n.1061G>A | ||
| ENST00000268124.9:c.863G>A | ENSP00000268124.5:p.Arg288His | |
| ENST00000442287.6:c.863G>A | ENSP00000399851.2:p.Arg288His | |
| ENST00000631044.2:c.*246G>A | ENSP00000486730.1:n.*246G>A | |
| NM_001126131.1:c.863G>A | NP_001119603.1:p.Arg288His | |
| NM_002693.2:c.863G>A | NP_002684.1:p.Arg288His | |
| NM_001126131.2:c.863G>A | NP_001119603.1:p.Arg288His | |
| NM_002693.3:c.863G>A MANE Select | NP_002684.1:p.Arg288His |