Linked Data
dbSNP Id:
rs2067005093
gnomAD v4:
17-36088393-G-T
MyVariant Identifiers:
chr17:g.34415739G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.36088393G>T , CM000679.2:g.36088393G>T | GRCh38 |
| NC_000017.10:g.34415739G>T , CM000679.1:g.34415739G>T | GRCh37 |
| NC_000017.9:g.31439852G>T | NCBI36 |
| NG_027730.1:g.6768C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613922.2:c.*279C>A (CCL3) MANE Select | ENSP00000477908.1:n.*279C>A | |
| ENST00000613922.1:c.*279C>A (CCL3) | ENSP00000477908.1:n.*279C>A | |
| ENST00000613928.1:n.1017C>A (CCL3) | ||
| ENST00000614051.1:n.1357C>A (CCL3) | ||
| NM_002983.2:c.*279C>A (CCL3) | NP_002974.1:n.*279C>A | |
| XR_001752857.1:n.1637-1153G>T (CCL3-AS1) | ||
| XR_001752858.1:n.673-1153G>T (CCL3-AS1) | ||
| XR_001752859.1:n.1584-1153G>T (CCL3-AS1) | ||
| NM_002983.3:c.*279C>A (CCL3) MANE Select | NP_002974.1:n.*279C>A | |
| NR_168494.1:n.1331C>A (CCL3) | ||
| NR_168495.1:n.541C>A (CCL3) | ||
| NR_168496.1:n.504C>A (CCL3) |