HGVS | Genome Assembly |
---|---|
NC_000017.11:g.36088260C>G , CM000679.2:g.36088260C>G | GRCh38 |
NC_000017.10:g.34415606C>G , CM000679.1:g.34415606C>G | GRCh37 |
NC_000017.9:g.31439719C>G | NCBI36 |
NG_027730.1:g.6901G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000613922.2:c.*412G>C (CCL3) MANE Select | ENSP00000477908.1:n.*412G>C | |
ENST00000613922.1:c.*412G>C (CCL3) | ENSP00000477908.1:n.*412G>C | |
ENST00000614051.1:n.1490G>C (CCL3) | ||
NM_002983.2:c.*412G>C (CCL3) | NP_002974.1:n.*412G>C | |
XR_001752857.1:n.1637-1286C>G (CCL3-AS1) | ||
XR_001752858.1:n.673-1286C>G (CCL3-AS1) | ||
XR_001752859.1:n.1584-1286C>G (CCL3-AS1) | ||
NM_002983.3:c.*412G>C (CCL3) MANE Select | NP_002974.1:n.*412G>C | |
NR_168494.1:n.1464G>C (CCL3) | ||
NR_168495.1:n.674G>C (CCL3) | ||
NR_168496.1:n.637G>C (CCL3) |