Canonical Allele Identifier: CA626206588
Gene: CCL3 HGNC NCBI
CCL3-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1388102905
gnomAD v2: 17-34415623-T-C
gnomAD v3: 17-36088277-T-C
gnomAD v4: 17-36088277-T-C
MyVariant Identifiers: chr17:g.34415623T>C (hg19) chr17:g.36088277T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.36088277T>C , CM000679.2:g.36088277T>C GRCh38
NC_000017.10:g.34415623T>C , CM000679.1:g.34415623T>C GRCh37
NC_000017.9:g.31439736T>C NCBI36
NG_027730.1:g.6884A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000613922.2:c.*395A>G (CCL3) MANE Select ENSP00000477908.1:n.*395A>G
ENST00000613922.1:c.*395A>G (CCL3) ENSP00000477908.1:n.*395A>G
ENST00000614051.1:n.1473A>G (CCL3)
NM_002983.2:c.*395A>G (CCL3) NP_002974.1:n.*395A>G
XR_001752857.1:n.1637-1269T>C (CCL3-AS1)
XR_001752858.1:n.673-1269T>C (CCL3-AS1)
XR_001752859.1:n.1584-1269T>C (CCL3-AS1)
NM_002983.3:c.*395A>G (CCL3) MANE Select NP_002974.1:n.*395A>G
NR_168494.1:n.1447A>G (CCL3)
NR_168495.1:n.657A>G (CCL3)
NR_168496.1:n.620A>G (CCL3)
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