Canonical Allele Identifier: CA499867183
Gene: CCL3 HGNC NCBI
CCL3-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2067006592
MyVariant Identifiers: chr17:g.34415830A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.36088484A>G , CM000679.2:g.36088484A>G GRCh38
NC_000017.10:g.34415830A>G , CM000679.1:g.34415830A>G GRCh37
NC_000017.9:g.31439943A>G NCBI36
NG_027730.1:g.6677T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000613922.2:c.*188T>C (CCL3) MANE Select ENSP00000477908.1:n.*188T>C
ENST00000613922.1:c.*188T>C (CCL3) ENSP00000477908.1:n.*188T>C
ENST00000613928.1:n.926T>C (CCL3)
ENST00000614051.1:n.1266T>C (CCL3)
NM_002983.2:c.*188T>C (CCL3) NP_002974.1:n.*188T>C
XR_001752857.1:n.1637-1062A>G (CCL3-AS1)
XR_001752858.1:n.673-1062A>G (CCL3-AS1)
XR_001752859.1:n.1584-1062A>G (CCL3-AS1)
NM_002983.3:c.*188T>C (CCL3) MANE Select NP_002974.1:n.*188T>C
NR_168494.1:n.1240T>C (CCL3)
NR_168495.1:n.450T>C (CCL3)
NR_168496.1:n.413T>C (CCL3)