Linked Data
ClinVar Variation Id:
996105
ClinVar RCV Id:
RCV001290389
dbSNP Id:
rs767693909
ExAC:
11:124742882 C / T
gnomAD v2:
11-124742882-C-T
gnomAD v4:
11-124872986-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.124872986C>T , CM000673.2:g.124872986C>T | GRCh38 |
| NC_000011.9:g.124742882C>T , CM000673.1:g.124742882C>T | GRCh37 |
| NC_000011.8:g.124248092C>T | NCBI36 |
| NG_016214.1:g.12578C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397801.6:c.1433C>T MANE Select | ENSP00000380903.1:p.Pro478Leu | |
| ENST00000397801.5:c.1433C>T | ENSP00000380903.1:p.Pro478Leu | |
| ENST00000538940.5:c.1367C>T | ENSP00000441797.1:p.Pro456Leu | |
| NM_022370.3:c.1433C>T | NP_071765.2:p.Pro478Leu | |
| XM_011542953.1:c.2405C>T | XP_011541255.1:p.Pro802Leu | |
| XM_017018122.1:c.1367C>T | XP_016873611.1:p.Pro456Leu | |
| NM_022370.4:c.1433C>T MANE Select | NP_071765.2:p.Pro478Leu |