Linked Data
MyVariant Identifiers:
chr17:g.45361828C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47284462C>G , CM000679.2:g.47284462C>G | GRCh38 |
| NC_000017.10:g.45361828C>G , CM000679.1:g.45361828C>G | GRCh37 |
| NC_000017.9:g.42716827C>G | NCBI36 |
| NG_008332.2:g.35621C>G , LRG_481:g.35621C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696963.1:c.381C>G | ENSP00000513002.1:p.Ser127= | |
| ENST00000559488.7:c.381C>G MANE Select | ENSP00000452786.2:p.Ser127= | |
| ENST00000559488.5:c.381C>G | ENSP00000452786.1:p.Ser127= | |
| ENST00000560629.1:c.346C>G | ||
| ENST00000571680.1:c.381C>G | ENSP00000461626.1:p.Ser127= | |
| NM_000212.2:c.381C>G , LRG_481t1:c.381C>G | NP_000203.2:p.Ser127= | |
| NM_000212.3:c.381C>G MANE Select | NP_000203.2:p.Ser127= |