Canonical Allele Identifier: CA983322138
Gene: CCL3 HGNC NCBI
CCL3-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2067006679
gnomAD v3: 17-36088485-CA-C
gnomAD v4: 17-36088485-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.36088490del , CM000679.2:g.36088490del GRCh38
NC_000017.10:g.34415836del , CM000679.1:g.34415836del GRCh37
NC_000017.9:g.31439949del NCBI36
NG_027730.1:g.6675del

Transcript Alleles

HGVS Amino-acid Change
ENST00000613922.2:c.*186del (CCL3) MANE Select ENSP00000477908.1:n.*186del
ENST00000613922.1:c.*186del (CCL3) ENSP00000477908.1:n.*186del
ENST00000613928.1:n.924del (CCL3)
ENST00000614051.1:n.1264del (CCL3)
NM_002983.2:c.*186del (CCL3) NP_002974.1:n.*186del
XR_001752857.1:n.1637-1056del (CCL3-AS1)
XR_001752858.1:n.673-1056del (CCL3-AS1)
XR_001752859.1:n.1584-1056del (CCL3-AS1)
NM_002983.3:c.*186del (CCL3) MANE Select NP_002974.1:n.*186del
NR_168494.1:n.1238del (CCL3)
NR_168495.1:n.448del (CCL3)
NR_168496.1:n.411del (CCL3)
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