Linked Data
gnomAD v4:
19-44949439-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.44949439C>A , CM000681.2:g.44949439C>A | GRCh38 |
| NC_000019.9:g.45452696C>A , CM000681.1:g.45452696C>A | GRCh37 |
| NC_000019.8:g.50144536C>A | NCBI36 |
| NG_008837.1:g.8454C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000252490.7:c.*190C>A (APOC2) MANE Select | ENSP00000252490.5:n.*190C>A | |
| ENST00000252490.5:c.*190C>A (APOC4-APOC2) | ENSP00000252490.4:n.*190C>A | |
| ENST00000585685.5:c.*1279C>A (APOC4-APOC2) | ENSP00000467185.1:n.*1279C>A | |
| ENST00000590360.2:c.*190C>A (APOC2) | ENSP00000466775.1:n.*190C>A | |
| NM_000483.4:c.*190C>A (APOC2) | NP_000474.2:n.*190C>A | |
| NR_037932.1:n.1703C>A (APOC4-APOC2) | ||
| NM_000483.5:c.*190C>A (APOC2) MANE Select | NP_000474.2:n.*190C>A |