Linked Data
dbSNP Id:
rs1478519359
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67585202C>G , CM000673.2:g.67585202C>G | GRCh38 |
| NC_000011.9:g.67352673C>G , CM000673.1:g.67352673C>G | GRCh37 |
| NC_000011.8:g.67109249C>G | NCBI36 |
| NG_012075.1:g.6608C>G , LRG_723:g.6608C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.297C>G | ENSP00000381604.1:p.Asp99Glu | |
| ENST00000398606.10:c.297C>G MANE Select | ENSP00000381607.3:p.Asp99Glu | |
| ENST00000646888.1:c.*13C>G | ENSP00000494477.1:n.*13C>G | |
| ENST00000398603.5:c.297C>G | ENSP00000381604.1:p.Asp99Glu | |
| ENST00000398606.7:c.297C>G | ENSP00000381607.3:p.Asp99Glu | |
| ENST00000467591.1:n.408C>G | ||
| ENST00000494593.1:n.1092C>G | ||
| ENST00000498765.5:c.360C>G | ||
| NM_000852.3:c.297C>G , LRG_723t1:c.297C>G | NP_000843.1:p.Asp99Glu | |
| NM_000852.4:c.297C>G MANE Select | NP_000843.1:p.Asp99Glu |