Linked Data
gnomAD v4:
17-36088278-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.36088278T>G , CM000679.2:g.36088278T>G | GRCh38 |
| NC_000017.10:g.34415624T>G , CM000679.1:g.34415624T>G | GRCh37 |
| NC_000017.9:g.31439737T>G | NCBI36 |
| NG_027730.1:g.6883A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613922.2:c.*394A>C (CCL3) MANE Select | ENSP00000477908.1:n.*394A>C | |
| ENST00000613922.1:c.*394A>C (CCL3) | ENSP00000477908.1:n.*394A>C | |
| ENST00000614051.1:n.1472A>C (CCL3) | ||
| NM_002983.2:c.*394A>C (CCL3) | NP_002974.1:n.*394A>C | |
| XR_001752857.1:n.1637-1268T>G (CCL3-AS1) | ||
| XR_001752858.1:n.673-1268T>G (CCL3-AS1) | ||
| XR_001752859.1:n.1584-1268T>G (CCL3-AS1) | ||
| NM_002983.3:c.*394A>C (CCL3) MANE Select | NP_002974.1:n.*394A>C | |
| NR_168494.1:n.1446A>C (CCL3) | ||
| NR_168495.1:n.656A>C (CCL3) | ||
| NR_168496.1:n.619A>C (CCL3) |