Linked Data
dbSNP Id:
rs1466865755
MyVariant Identifiers:
chr19:g.45452345_45452346insTCT (hg19)
chr19:g.44949088_44949089insTCT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.44949090_44949091insTTC , CM000681.2:g.44949090_44949091insTTC | GRCh38 |
| NC_000019.9:g.45452347_45452348insTTC , CM000681.1:g.45452347_45452348insTTC | GRCh37 |
| NC_000019.8:g.50144187_50144188insTTC | NCBI36 |
| NG_008837.1:g.8105_8106insTTC |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000252490.7:c.216-69_216-68insTTC (APOC2) MANE Select | ENSP00000252490.5:n.216-69_216-68insTTC | |
| ENST00000252490.5:c.216-69_216-68insTTC (APOC4-APOC2) | ENSP00000252490.4:n.216-69_216-68insTTC | |
| ENST00000585685.5:c.*999-69_*999-68insTTC (APOC4-APOC2) | ENSP00000467185.1:n.*999-69_*999-68insTTC... | |
| ENST00000585786.1:c.*226_*227insTTC (APOC2) | ENSP00000465001.1:n.*226_*227insTTC | |
| ENST00000589057.5:c.447-69_447-68insTTC (APOC4-APOC2) | ENSP00000468139.1:n.447-69_447-68insTTC | |
| ENST00000590360.2:c.216-69_216-68insTTC (APOC2) | ENSP00000466775.1:n.216-69_216-68insTTC | |
| ENST00000591597.5:c.174-69_174-68insTTC (APOC2) | ENSP00000476835.1:n.174-69_174-68insTTC | |
| ENST00000592257.5:c.*10-69_*10-68insTTC (APOC2) | ENSP00000477261.1:n.*10-69_*10-68insTTC | |
| NM_000483.4:c.216-69_216-68insTTC (APOC2) | NP_000474.2:n.216-69_216-68insTTC | |
| NR_037932.1:n.1423-69_1423-68insTTC (APOC4-APOC2) | ||
| NM_000483.5:c.216-69_216-68insTTC (APOC2) MANE Select | NP_000474.2:n.216-69_216-68insTTC |