Linked Data
ClinVar Variation Id:
10206
ClinVar RCV Id:
RCV000010919
dbSNP Id:
rs28933669
PubMed:
PMID:8052958
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154966523A>G , CM000685.2:g.154966523A>G | GRCh38 |
| NC_000023.10:g.154194798A>G , CM000685.1:g.154194798A>G | GRCh37 |
| NC_000023.9:g.153847992A>G | NCBI36 |
| NG_011403.1:g.61201T>C | |
| NG_011403.2:g.61201T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.1174T>C MANE Select | ENSP00000353393.4:p.Ser392Pro | |
| ENST00000647125.1:c.*1050T>C | ENSP00000496062.1:n.*1050T>C | |
| ENST00000360256.8:c.1174T>C | ENSP00000353393.4:p.Ser392Pro | |
| NM_000132.3:c.1174T>C | NP_000123.1:p.Ser392Pro | |
| XM_011531126.1:c.1069T>C | XP_011529428.1:p.Ser357Pro | |
| NM_000132.4:c.1174T>C MANE Select | NP_000123.1:p.Ser392Pro |