MyVariant.info:
GRCh37
chr19:g.45451741C>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.44948484C>A , CM000681.2:g.44948484C>A | GRCh38 |
| NC_000019.9:g.45451741C>A , CM000681.1:g.45451741C>A | GRCh37 |
| NC_000019.8:g.50143581C>A | NCBI36 |
| NG_008837.1:g.7499C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252490.7:c.6C>A (APOC2) MANE Select | ENSP00000252490.5:p.Gly2= | |
| ENST00000252490.5:c.6C>A (APOC4-APOC2) | ENSP00000252490.4:p.Gly2= | |
| ENST00000585685.5:c.*789C>A (APOC4-APOC2) | ENSP00000467185.1:n.*789C>A | |
| ENST00000585786.1:c.6C>A (APOC2) | ENSP00000465001.1:p.Gly2= | |
| ENST00000589057.5:c.237C>A (APOC4-APOC2) | ENSP00000468139.1:p.Gly79= | |
| ENST00000590360.2:c.6C>A (APOC2) | ENSP00000466775.1:p.Gly2= | |
| ENST00000591597.5:c.6C>A (APOC2) | ENSP00000476835.1:p.Gly2= | |
| ENST00000592257.5:c.6C>A (APOC2) | ENSP00000477261.1:p.Gly2= | |
| NM_000483.4:c.6C>A (APOC2) | NP_000474.2:p.Gly2= | |
| NR_037932.1:n.1213C>A (APOC4-APOC2) | ||
| NM_000483.5:c.6C>A (APOC2) MANE Select | NP_000474.2:p.Gly2= |