gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00000705 (SAS)
Exomes Max Group AF
0.00000432 (NFE)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.36088473G>A , CM000679.2:g.36088473G>A | GRCh38 |
| NC_000017.10:g.34415819G>A , CM000679.1:g.34415819G>A | GRCh37 |
| NC_000017.9:g.31439932G>A | NCBI36 |
| NG_027730.1:g.6688C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613922.2:c.*199C>T (CCL3) MANE Select | ENSP00000477908.1:n.*199C>T | |
| ENST00000613922.1:c.*199C>T (CCL3) | ENSP00000477908.1:n.*199C>T | |
| ENST00000613928.1:n.937C>T (CCL3) | ||
| ENST00000614051.1:n.1277C>T (CCL3) | ||
| NM_002983.2:c.*199C>T (CCL3) | NP_002974.1:n.*199C>T | |
| XR_001752857.1:n.1637-1073G>A (CCL3-AS1) | ||
| XR_001752858.1:n.673-1073G>A (CCL3-AS1) | ||
| XR_001752859.1:n.1584-1073G>A (CCL3-AS1) | ||
| NM_002983.3:c.*199C>T (CCL3) MANE Select | NP_002974.1:n.*199C>T | |
| NR_168494.1:n.1251C>T (CCL3) | ||
| NR_168495.1:n.461C>T (CCL3) | ||
| NR_168496.1:n.424C>T (CCL3) |