Linked Data
gnomAD v4:
19-44949473-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.44949473T>C , CM000681.2:g.44949473T>C | GRCh38 |
| NC_000019.9:g.45452730T>C , CM000681.1:g.45452730T>C | GRCh37 |
| NC_000019.8:g.50144570T>C | NCBI36 |
| NG_008837.1:g.8488T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252490.7:c.*224T>C (APOC2) MANE Select | ENSP00000252490.5:n.*224T>C | |
| ENST00000252490.5:c.*224T>C (APOC4-APOC2) | ENSP00000252490.4:n.*224T>C | |
| ENST00000585685.5:c.*1313T>C (APOC4-APOC2) | ENSP00000467185.1:n.*1313T>C | |
| ENST00000590360.2:c.*224T>C (APOC2) | ENSP00000466775.1:n.*224T>C | |
| NM_000483.4:c.*224T>C (APOC2) | NP_000474.2:n.*224T>C | |
| NR_037932.1:n.1737T>C (APOC4-APOC2) | ||
| NM_000483.5:c.*224T>C (APOC2) MANE Select | NP_000474.2:n.*224T>C |