HGVS | Genome Assembly |
---|---|
NC_000019.10:g.44949452G>C , CM000681.2:g.44949452G>C | GRCh38 |
NC_000019.9:g.45452709G>C , CM000681.1:g.45452709G>C | GRCh37 |
NC_000019.8:g.50144549G>C | NCBI36 |
NG_008837.1:g.8467G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000252490.7:c.*203G>C (APOC2) MANE Select | ENSP00000252490.5:n.*203G>C | |
ENST00000252490.5:c.*203G>C (APOC4-APOC2) | ENSP00000252490.4:n.*203G>C | |
ENST00000585685.5:c.*1292G>C (APOC4-APOC2) | ENSP00000467185.1:n.*1292G>C | |
ENST00000590360.2:c.*203G>C (APOC2) | ENSP00000466775.1:n.*203G>C | |
NM_000483.4:c.*203G>C (APOC2) | NP_000474.2:n.*203G>C | |
NR_037932.1:n.1716G>C (APOC4-APOC2) | ||
NM_000483.5:c.*203G>C (APOC2) MANE Select | NP_000474.2:n.*203G>C |