Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.99985646C>G , CM000675.2:g.99985646C>G | GRCh38 |
| NC_000013.10:g.100637900C>G , CM000675.1:g.100637900C>G | GRCh37 |
| NC_000013.9:g.99435901C>G | NCBI36 |
| NG_007085.2:g.8582C>G | |
| NG_007085.3:g.8891C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376335.8:c.1563C>G MANE Select | ENSP00000365514.3:p.Ser521Arg | |
| ENST00000376335.7:c.1563C>G | ENSP00000365514.3:p.Ser521Arg | |
| ENST00000481565.1:n.153C>G | ||
| ENST00000620342.1:c.1560C>G | ENSP00000481510.1:p.Ser520Arg | |
| NM_007129.3:c.1563C>G | NP_009060.2:p.Ser521Arg | |
| NM_007129.4:c.1563C>G | NP_009060.2:p.Ser521Arg | |
| NM_007129.5:c.1563C>G MANE Select | NP_009060.2:p.Ser521Arg |