HGVS | Genome Assembly |
---|---|
NC_000019.10:g.44949466G>A , CM000681.2:g.44949466G>A | GRCh38 |
NC_000019.9:g.45452723G>A , CM000681.1:g.45452723G>A | GRCh37 |
NC_000019.8:g.50144563G>A | NCBI36 |
NG_008837.1:g.8481G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252490.7:c.*217G>A (APOC2) MANE Select | ENSP00000252490.5:n.*217G>A | |
ENST00000252490.5:c.*217G>A (APOC4-APOC2) | ENSP00000252490.4:n.*217G>A | |
ENST00000585685.5:c.*1306G>A (APOC4-APOC2) | ENSP00000467185.1:n.*1306G>A | |
ENST00000590360.2:c.*217G>A (APOC2) | ENSP00000466775.1:n.*217G>A | |
NM_000483.4:c.*217G>A (APOC2) | NP_000474.2:n.*217G>A | |
NR_037932.1:n.1730G>A (APOC4-APOC2) | ||
NM_000483.5:c.*217G>A (APOC2) MANE Select | NP_000474.2:n.*217G>A |