Linked Data
gnomAD v4:
19-44949198-C-T
COSMIC:
COSM4944576
MyVariant Identifiers:
chr19:g.45452455C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.44949198C>T , CM000681.2:g.44949198C>T | GRCh38 |
| NC_000019.9:g.45452455C>T , CM000681.1:g.45452455C>T | GRCh37 |
| NC_000019.8:g.50144295C>T | NCBI36 |
| NG_008837.1:g.8213C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000252490.7:c.255C>T (APOC2) MANE Select | ENSP00000252490.5:p.Tyr85= | |
| ENST00000252490.5:c.255C>T (APOC4-APOC2) | ENSP00000252490.4:p.Tyr85= | |
| ENST00000585685.5:c.*1038C>T (APOC4-APOC2) | ENSP00000467185.1:n.*1038C>T | |
| ENST00000585786.1:c.*334C>T (APOC2) | ENSP00000465001.1:n.*334C>T | |
| ENST00000589057.5:c.486C>T (APOC4-APOC2) | ENSP00000468139.1:p.Tyr162= | |
| ENST00000590360.2:c.255C>T (APOC2) | ENSP00000466775.1:p.Tyr85= | |
| ENST00000591597.5:c.213C>T (APOC2) | ENSP00000476835.1:p.Tyr71= | |
| ENST00000592257.5:c.*49C>T (APOC2) | ENSP00000477261.1:n.*49C>T | |
| NM_000483.4:c.255C>T (APOC2) | NP_000474.2:p.Tyr85= | |
| NR_037932.1:n.1462C>T (APOC4-APOC2) | ||
| NM_000483.5:c.255C>T (APOC2) MANE Select | NP_000474.2:p.Tyr85= |