Linked Data
dbSNP Id:
rs1427025352
gnomAD v2:
17-34415735-G-A
gnomAD v3:
17-36088389-G-A
gnomAD v4:
17-36088389-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.36088389G>A , CM000679.2:g.36088389G>A | GRCh38 |
| NC_000017.10:g.34415735G>A , CM000679.1:g.34415735G>A | GRCh37 |
| NC_000017.9:g.31439848G>A | NCBI36 |
| NG_027730.1:g.6772C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613922.2:c.*283C>T (CCL3) MANE Select | ENSP00000477908.1:n.*283C>T | |
| ENST00000613922.1:c.*283C>T (CCL3) | ENSP00000477908.1:n.*283C>T | |
| ENST00000613928.1:n.1021C>T (CCL3) | ||
| ENST00000614051.1:n.1361C>T (CCL3) | ||
| NM_002983.2:c.*283C>T (CCL3) | NP_002974.1:n.*283C>T | |
| XR_001752857.1:n.1637-1157G>A (CCL3-AS1) | ||
| XR_001752858.1:n.673-1157G>A (CCL3-AS1) | ||
| XR_001752859.1:n.1584-1157G>A (CCL3-AS1) | ||
| NM_002983.3:c.*283C>T (CCL3) MANE Select | NP_002974.1:n.*283C>T | |
| NR_168494.1:n.1335C>T (CCL3) | ||
| NR_168495.1:n.545C>T (CCL3) | ||
| NR_168496.1:n.508C>T (CCL3) |