Linked Data
ClinVar Variation Id:
13189
ClinVar RCV Id:
RCV000014077
dbSNP Id:
rs28933391
PubMed:
PMID:15138885
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.58428084G>A , CM000665.2:g.58428084G>A | GRCh38 |
| NC_000003.11:g.58413811G>A , CM000665.1:g.58413811G>A | GRCh37 |
| NC_000003.10:g.58388851G>A | NCBI36 |
| NG_016860.1:g.10769C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000302746.11:c.1030C>T MANE Select | ENSP00000307241.6:p.Pro344Ser | |
| ENST00000302746.10:c.1030C>T | ENSP00000307241.6:p.Pro344Ser | |
| ENST00000383714.8:c.976C>T | ENSP00000373220.4:p.Pro326Ser | |
| ENST00000461692.5:n.1143C>T | ||
| ENST00000469364.5:c.*416C>T | ENSP00000419580.1:n.*416C>T | |
| ENST00000474765.1:c.*44C>T | ENSP00000418448.1:n.*44C>T | |
| ENST00000479945.1:n.4056C>T | ||
| ENST00000485460.5:c.976C>T | ENSP00000417267.1:p.Pro326Ser | |
| NM_000925.3:c.1030C>T | NP_000916.2:p.Pro344Ser | |
| NM_001173468.1:c.976C>T | NP_001166939.1:p.Pro326Ser | |
| NM_001315536.1:c.976C>T | NP_001302465.1:p.Pro326Ser | |
| NR_033384.1:n.1143C>T | ||
| NM_000925.4:c.1030C>T MANE Select | NP_000916.2:p.Pro344Ser | |
| NM_001173468.2:c.976C>T | NP_001166939.1:p.Pro326Ser | |
| NM_001315536.2:c.976C>T | NP_001302465.1:p.Pro326Ser | |
| NR_033384.2:n.1136C>T |