Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.36088284T>A , CM000679.2:g.36088284T>A | GRCh38 |
| NC_000017.10:g.34415630T>A , CM000679.1:g.34415630T>A | GRCh37 |
| NC_000017.9:g.31439743T>A | NCBI36 |
| NG_027730.1:g.6877A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613922.2:c.*388A>T (CCL3) MANE Select | ENSP00000477908.1:n.*388A>T | |
| ENST00000613922.1:c.*388A>T (CCL3) | ENSP00000477908.1:n.*388A>T | |
| ENST00000614051.1:n.1466A>T (CCL3) | ||
| NM_002983.2:c.*388A>T (CCL3) | NP_002974.1:n.*388A>T | |
| XR_001752857.1:n.1637-1262T>A (CCL3-AS1) | ||
| XR_001752858.1:n.673-1262T>A (CCL3-AS1) | ||
| XR_001752859.1:n.1584-1262T>A (CCL3-AS1) | ||
| NM_002983.3:c.*388A>T (CCL3) MANE Select | NP_002974.1:n.*388A>T | |
| NR_168494.1:n.1440A>T (CCL3) | ||
| NR_168495.1:n.650A>T (CCL3) | ||
| NR_168496.1:n.613A>T (CCL3) |