Linked Data
dbSNP Id:
rs1261293361
gnomAD v2:
17-34415733-T-TCGGTTGTCA
gnomAD v3:
17-36088387-T-TCGGTTGTCA
gnomAD v4:
17-36088387-T-TCGGTTGTCA
MyVariant Identifiers:
chr17:g.34415733_34415734insCGGTTGTCA (hg19)
chr17:g.36088387_36088388insCGGTTGTCA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.36088389_36088397dup , CM000679.2:g.36088389_36088397dup | GRCh38 |
| NC_000017.10:g.34415735_34415743dup , CM000679.1:g.34415735_34415743dup | GRCh37 |
| NC_000017.9:g.31439848_31439856dup | NCBI36 |
| NG_027730.1:g.6765_6773dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613922.2:c.*276_*284dup (CCL3) MANE Select | ENSP00000477908.1:n.*276_*284dup | |
| ENST00000613922.1:c.*276_*284dup (CCL3) | ENSP00000477908.1:n.*276_*284dup | |
| ENST00000613928.1:n.1014_1022dup (CCL3) | ||
| ENST00000614051.1:n.1354_1362dup (CCL3) | ||
| NM_002983.2:c.*276_*284dup (CCL3) | NP_002974.1:n.*276_*284dup | |
| XR_001752857.1:n.1637-1157_1637-1149dup (CCL3-AS1) | ||
| XR_001752858.1:n.673-1157_673-1149dup (CCL3-AS1) | ||
| XR_001752859.1:n.1584-1157_1584-1149dup (CCL3-AS1) | ||
| NM_002983.3:c.*276_*284dup (CCL3) MANE Select | NP_002974.1:n.*276_*284dup | |
| NR_168494.1:n.1328_1336dup (CCL3) | ||
| NR_168495.1:n.538_546dup (CCL3) | ||
| NR_168496.1:n.501_509dup (CCL3) |