Linked Data
ClinVar Variation Id:
261250
dbSNP Id:
rs150385364
ExAC:
11:824021 C / T
gnomAD v2:
11-824021-C-T
gnomAD v3:
11-824021-C-T
gnomAD v4:
11-824021-C-T
PubMed:
PMID:28135719
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.824021C>T , CM000673.2:g.824021C>T | GRCh38 |
| NC_000011.9:g.824021C>T , CM000673.1:g.824021C>T | GRCh37 |
| NC_000011.8:g.814021C>T | NCBI36 |
| NG_023394.1:g.10121C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000336615.9:c.943C>T MANE Select | ENSP00000337701.4:p.Pro315Ser | |
| ENST00000336615.8:c.943C>T | ENSP00000337701.4:p.Pro315Ser | |
| ENST00000525250.5:n.1797C>T | ||
| ENST00000526083.1:n.232C>T | ||
| ENST00000529255.1:n.373C>T | ||
| ENST00000617551.1:c.-60C>T | ENSP00000481602.1:n.-60C>T | |
| NM_020376.3:c.943C>T | NP_065109.1:p.Pro315Ser | |
| XM_006718265.2:c.1085C>T | XP_006718328.1:p.Ala362Val | |
| XM_006718266.2:c.1085C>T | XP_006718329.1:p.Ala362Val | |
| XM_006718265.3:c.1085C>T | XP_006718328.1:p.Ala362Val | |
| XM_006718266.3:c.1085C>T | XP_006718329.1:p.Ala362Val | |
| XM_017018028.1:c.943C>T | XP_016873517.1:p.Pro315Ser | |
| XM_024448618.1:c.1085C>T | XP_024304386.1:p.Ala362Val | |
| NM_020376.4:c.943C>T MANE Select | NP_065109.1:p.Pro315Ser |