Linked Data
ClinVar Variation Id:
957393
ClinVar RCV Id:
RCV001230364
dbSNP Id:
rs1313908557
gnomAD v4:
14-28767604-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.28767604C>A , CM000676.2:g.28767604C>A | GRCh38 |
| NC_000014.8:g.29236810C>A , CM000676.1:g.29236810C>A | GRCh37 |
| NC_000014.7:g.28306561C>A | NCBI36 |
| NG_009367.1:g.5524C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706482.1:c.325C>A | ENSP00000516406.1:p.Pro109Thr | |
| ENST00000313071.7:c.325C>A MANE Select | ENSP00000339004.3:p.Pro109Thr | |
| ENST00000313071.6:c.325C>A | ENSP00000339004.3:p.Pro109Thr | |
| NM_005249.4:c.325C>A | NP_005240.3:p.Pro109Thr | |
| NM_005249.5:c.325C>A MANE Select | NP_005240.3:p.Pro109Thr |