HGVS | Genome Assembly |
---|---|
NC_000017.11:g.36088282T= , CM000679.2:g.36088282T= | GRCh38 |
NC_000017.10:g.34415628T= , CM000679.1:g.34415628T= | GRCh37 |
NC_000017.9:g.31439741T= | NCBI36 |
NG_027730.1:g.6879A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000613922.2:c.*390A= (CCL3) MANE Select | ENSP00000477908.1:n.*390A= | |
ENST00000613922.1:c.*390A= (CCL3) | ENSP00000477908.1:n.*390A= | |
ENST00000614051.1:n.1468A= (CCL3) | ||
NM_002983.2:c.*390A= (CCL3) | NP_002974.1:n.*390A= | |
XR_001752857.1:n.1637-1264T= (CCL3-AS1) | ||
XR_001752858.1:n.673-1264T= (CCL3-AS1) | ||
XR_001752859.1:n.1584-1264T= (CCL3-AS1) | ||
NM_002983.3:c.*390A= (CCL3) MANE Select | NP_002974.1:n.*390A= | |
NR_168494.1:n.1442A= (CCL3) | ||
NR_168495.1:n.652A= (CCL3) | ||
NR_168496.1:n.615A= (CCL3) |