Linked Data
dbSNP Id:
rs1301555431
gnomAD v2:
17-34415629-A-G
gnomAD v3:
17-36088283-A-G
gnomAD v4:
17-36088283-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.36088283A>G , CM000679.2:g.36088283A>G | GRCh38 |
| NC_000017.10:g.34415629A>G , CM000679.1:g.34415629A>G | GRCh37 |
| NC_000017.9:g.31439742A>G | NCBI36 |
| NG_027730.1:g.6878T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613922.2:c.*389T>C (CCL3) MANE Select | ENSP00000477908.1:n.*389T>C | |
| ENST00000613922.1:c.*389T>C (CCL3) | ENSP00000477908.1:n.*389T>C | |
| ENST00000614051.1:n.1467T>C (CCL3) | ||
| NM_002983.2:c.*389T>C (CCL3) | NP_002974.1:n.*389T>C | |
| XR_001752857.1:n.1637-1263A>G (CCL3-AS1) | ||
| XR_001752858.1:n.673-1263A>G (CCL3-AS1) | ||
| XR_001752859.1:n.1584-1263A>G (CCL3-AS1) | ||
| NM_002983.3:c.*389T>C (CCL3) MANE Select | NP_002974.1:n.*389T>C | |
| NR_168494.1:n.1441T>C (CCL3) | ||
| NR_168495.1:n.651T>C (CCL3) | ||
| NR_168496.1:n.614T>C (CCL3) |