MyVariant.info:
GRCh37
chr19:g.45452458A>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.44949201A>G , CM000681.2:g.44949201A>G | GRCh38 |
| NC_000019.9:g.45452458A>G , CM000681.1:g.45452458A>G | GRCh37 |
| NC_000019.8:g.50144298A>G | NCBI36 |
| NG_008837.1:g.8216A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252490.7:c.258A>G (APOC2) MANE Select | ENSP00000252490.5:p.Thr86= | |
| ENST00000252490.5:c.258A>G (APOC4-APOC2) | ENSP00000252490.4:p.Thr86= | |
| ENST00000585685.5:c.*1041A>G (APOC4-APOC2) | ENSP00000467185.1:n.*1041A>G | |
| ENST00000585786.1:c.*337A>G (APOC2) | ENSP00000465001.1:n.*337A>G | |
| ENST00000589057.5:c.489A>G (APOC4-APOC2) | ENSP00000468139.1:p.Thr163= | |
| ENST00000590360.2:c.258A>G (APOC2) | ENSP00000466775.1:p.Thr86= | |
| ENST00000591597.5:c.216A>G (APOC2) | ENSP00000476835.1:p.Thr72= | |
| ENST00000592257.5:c.*52A>G (APOC2) | ENSP00000477261.1:n.*52A>G | |
| NM_000483.4:c.258A>G (APOC2) | NP_000474.2:p.Thr86= | |
| NR_037932.1:n.1465A>G (APOC4-APOC2) | ||
| NM_000483.5:c.258A>G (APOC2) MANE Select | NP_000474.2:p.Thr86= |