HGVS | Genome Assembly |
---|---|
NC_000017.11:g.36088274A>G , CM000679.2:g.36088274A>G | GRCh38 |
NC_000017.10:g.34415620A>G , CM000679.1:g.34415620A>G | GRCh37 |
NC_000017.9:g.31439733A>G | NCBI36 |
NG_027730.1:g.6887T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000613922.2:c.*398T>C (CCL3) MANE Select | ENSP00000477908.1:n.*398T>C | |
ENST00000613922.1:c.*398T>C (CCL3) | ENSP00000477908.1:n.*398T>C | |
ENST00000614051.1:n.1476T>C (CCL3) | ||
NM_002983.2:c.*398T>C (CCL3) | NP_002974.1:n.*398T>C | |
XR_001752857.1:n.1637-1272A>G (CCL3-AS1) | ||
XR_001752858.1:n.673-1272A>G (CCL3-AS1) | ||
XR_001752859.1:n.1584-1272A>G (CCL3-AS1) | ||
NM_002983.3:c.*398T>C (CCL3) MANE Select | NP_002974.1:n.*398T>C | |
NR_168494.1:n.1450T>C (CCL3) | ||
NR_168495.1:n.660T>C (CCL3) | ||
NR_168496.1:n.623T>C (CCL3) |