HGVS | Genome Assembly |
---|---|
NC_000019.10:g.44949396G= , CM000681.2:g.44949396G= | GRCh38 |
NC_000019.9:g.45452653G= , CM000681.1:g.45452653G= | GRCh37 |
NC_000019.8:g.50144493G= | NCBI36 |
NG_008837.1:g.8411G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252490.7:c.*147G= (APOC2) MANE Select | ENSP00000252490.5:n.*147G= | |
ENST00000252490.5:c.*147G= (APOC4-APOC2) | ENSP00000252490.4:n.*147G= | |
ENST00000585685.5:c.*1236G= (APOC4-APOC2) | ENSP00000467185.1:n.*1236G= | |
ENST00000590360.2:c.*147G= (APOC2) | ENSP00000466775.1:n.*147G= | |
ENST00000591597.5:c.*147G= (APOC2) | ENSP00000476835.1:n.*147G= | |
NM_000483.4:c.*147G= (APOC2) | NP_000474.2:n.*147G= | |
NR_037932.1:n.1660G= (APOC4-APOC2) | ||
NM_000483.5:c.*147G= (APOC2) MANE Select | NP_000474.2:n.*147G= |