Canonical Allele Identifier: CA499866800
Gene: CCL3 HGNC NCBI
CCL3-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2067004237
MyVariant Identifiers: chr17:g.34415697G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.36088351G>T , CM000679.2:g.36088351G>T GRCh38
NC_000017.10:g.34415697G>T , CM000679.1:g.34415697G>T GRCh37
NC_000017.9:g.31439810G>T NCBI36
NG_027730.1:g.6810C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000613922.2:c.*321C>A (CCL3) MANE Select ENSP00000477908.1:n.*321C>A
ENST00000613922.1:c.*321C>A (CCL3) ENSP00000477908.1:n.*321C>A
ENST00000613928.1:n.1059C>A (CCL3)
ENST00000614051.1:n.1399C>A (CCL3)
NM_002983.2:c.*321C>A (CCL3) NP_002974.1:n.*321C>A
XR_001752857.1:n.1637-1195G>T (CCL3-AS1)
XR_001752858.1:n.673-1195G>T (CCL3-AS1)
XR_001752859.1:n.1584-1195G>T (CCL3-AS1)
NM_002983.3:c.*321C>A (CCL3) MANE Select NP_002974.1:n.*321C>A
NR_168494.1:n.1373C>A (CCL3)
NR_168495.1:n.583C>A (CCL3)
NR_168496.1:n.546C>A (CCL3)