Linked Data
dbSNP Id:
rs753104405
gnomAD v2:
17-34415946-C-T
gnomAD v3:
17-36088600-C-T
gnomAD v4:
17-36088600-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.36088600C>T , CM000679.2:g.36088600C>T | GRCh38 |
| NC_000017.10:g.34415946C>T , CM000679.1:g.34415946C>T | GRCh37 |
| NC_000017.9:g.31440059C>T | NCBI36 |
| NG_027730.1:g.6561G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613922.2:c.*72G>A (CCL3) MANE Select | ENSP00000477908.1:n.*72G>A | |
| ENST00000613922.1:c.*72G>A (CCL3) | ENSP00000477908.1:n.*72G>A | |
| ENST00000613928.1:n.810G>A (CCL3) | ||
| ENST00000614051.1:n.1150G>A (CCL3) | ||
| NM_002983.2:c.*72G>A (CCL3) | NP_002974.1:n.*72G>A | |
| XR_001752857.1:n.1637-946C>T (CCL3-AS1) | ||
| XR_001752858.1:n.673-946C>T (CCL3-AS1) | ||
| XR_001752859.1:n.1584-946C>T (CCL3-AS1) | ||
| NM_002983.3:c.*72G>A (CCL3) MANE Select | NP_002974.1:n.*72G>A | |
| NR_168494.1:n.1124G>A (CCL3) | ||
| NR_168495.1:n.334G>A (CCL3) | ||
| NR_168496.1:n.297G>A (CCL3) |