Linked Data
ClinVar Variation Id:
2139533
dbSNP Id:
rs549092966
ExAC:
15:42693839 A / G
gnomAD v2:
15-42693839-A-G
gnomAD v3:
15-42401641-A-G
gnomAD v4:
15-42401641-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.42401641A>G , CM000677.2:g.42401641A>G | GRCh38 |
| NC_000015.9:g.42693839A>G , CM000677.1:g.42693839A>G | GRCh37 |
| NC_000015.8:g.40481131A>G | NCBI36 |
| NG_008660.1:g.58539A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349748.8:c.1211A>G | ENSP00000183936.4:p.Asp404Gly | |
| ENST00000357568.8:c.1355A>G | ENSP00000350181.3:p.Asp452Gly | |
| ENST00000397163.8:c.1355A>G MANE Select | ENSP00000380349.3:p.Asp452Gly | |
| ENST00000466369.5:n.1864A>G | ||
| ENST00000483208.5:n.1586A>G | ||
| ENST00000495723.1:n.1586A>G | ||
| ENST00000549793.5:n.1586A>G | ||
| ENST00000638141.2:n.1226A>G | ||
| ENST00000673705.1:c.309+1989A>G | ENSP00000501021.1:n.309+1989A>G | |
| ENST00000318023.11:c.1211A>G | ENSP00000326281.8:p.Asp404Gly | |
| ENST00000349748.7:c.1211A>G | ENSP00000183936.4:p.Asp404Gly | |
| ENST00000357568.7:c.1355A>G | ENSP00000350181.3:p.Asp452Gly | |
| ENST00000397163.7:c.1355A>G | ENSP00000380349.3:p.Asp452Gly | |
| NM_000070.2:c.1355A>G | NP_000061.1:p.Asp452Gly | |
| NM_024344.1:c.1355A>G | NP_077320.1:p.Asp452Gly | |
| NM_173087.1:c.1211A>G | NP_775110.1:p.Asp404Gly | |
| NM_000070.3:c.1355A>G MANE Select | NP_000061.1:p.Asp452Gly | |
| NM_024344.2:c.1355A>G | NP_077320.1:p.Asp452Gly | |
| NM_173087.2:c.1211A>G | NP_775110.1:p.Asp404Gly |