Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.36088290C= , CM000679.2:g.36088290C= | GRCh38 |
| NC_000017.10:g.34415636C= , CM000679.1:g.34415636C= | GRCh37 |
| NC_000017.9:g.31439749C= | NCBI36 |
| NG_027730.1:g.6871G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613922.2:c.*382G= (CCL3) MANE Select | ENSP00000477908.1:n.*382G= | |
| ENST00000613922.1:c.*382G= (CCL3) | ENSP00000477908.1:n.*382G= | |
| ENST00000614051.1:n.1460G= (CCL3) | ||
| NM_002983.2:c.*382G= (CCL3) | NP_002974.1:n.*382G= | |
| XR_001752857.1:n.1637-1256C= (CCL3-AS1) | ||
| XR_001752858.1:n.673-1256C= (CCL3-AS1) | ||
| XR_001752859.1:n.1584-1256C= (CCL3-AS1) | ||
| NM_002983.3:c.*382G= (CCL3) MANE Select | NP_002974.1:n.*382G= | |
| NR_168494.1:n.1434G= (CCL3) | ||
| NR_168495.1:n.644G= (CCL3) | ||
| NR_168496.1:n.607G= (CCL3) |