Linked Data
ClinVar Variation Id:
65896
ClinVar RCV Id:
RCV000056141
dbSNP Id:
rs587778808
gnomAD v4:
2-218812657-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218812657C>A , CM000664.2:g.218812657C>A | GRCh38 |
| NC_000002.11:g.219677380C>A , CM000664.1:g.219677380C>A | GRCh37 |
| NC_000002.10:g.219385624C>A | NCBI36 |
| NG_007959.1:g.35909C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258415.9:c.752C>A MANE Select | ENSP00000258415.4:p.Ser251Ter | |
| ENST00000258415.8:c.752C>A | ENSP00000258415.4:p.Ser251Ter | |
| ENST00000411688.1:c.470C>A | ENSP00000392671.1:p.Ser157Ter | |
| ENST00000445971.1:c.*213C>A | ENSP00000404945.1:n.*213C>A | |
| ENST00000466602.1:n.700C>A | ||
| ENST00000494263.5:n.1186C>A | ||
| NM_000784.3:c.752C>A | NP_000775.1:p.Ser251Ter | |
| XM_017003488.2:c.332C>A | XP_016858977.1:p.Ser111Ter | |
| NM_000784.4:c.752C>A MANE Select | NP_000775.1:p.Ser251Ter |