Linked Data
ClinVar Variation Id:
925777
ClinVar RCV Id:
RCV001187942
dbSNP Id:
rs958750957
gnomAD v4:
1-55039926-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.55039926C>A , CM000663.2:g.55039926C>A | GRCh38 |
| NC_000001.10:g.55505599C>A , CM000663.1:g.55505599C>A | GRCh37 |
| NC_000001.9:g.55278187C>A | NCBI36 |
| NG_009061.1:g.5380C>A , LRG_275:g.5380C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673913.2:c.89C>A | ENSP00000501161.2:p.Ala30Glu | |
| ENST00000710286.1:c.446C>A | ENSP00000518176.1:p.Ala149Glu | |
| ENST00000673726.1:c.89C>A | ENSP00000501004.1:p.Ala30Glu | |
| ENST00000302118.5:c.89C>A MANE Select | ENSP00000303208.5:p.Ala30Glu | |
| NM_174936.3:c.89C>A , LRG_275t1:c.89C>A | NP_777596.2:p.Ala30Glu | |
| NM_174936.4:c.89C>A MANE Select | NP_777596.2:p.Ala30Glu |