Canonical Allele Identifier: CA499866639
Gene: CCL3 HGNC NCBI
CCL3-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1444699050

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.36088295C>T , CM000679.2:g.36088295C>T GRCh38
NC_000017.10:g.34415641C>T , CM000679.1:g.34415641C>T GRCh37
NC_000017.9:g.31439754C>T NCBI36
NG_027730.1:g.6866G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000613922.2:c.*377G>A (CCL3) MANE Select ENSP00000477908.1:n.*377G>A
ENST00000613922.1:c.*377G>A (CCL3) ENSP00000477908.1:n.*377G>A
ENST00000613928.1:n.1115G>A (CCL3)
ENST00000614051.1:n.1455G>A (CCL3)
NM_002983.2:c.*377G>A (CCL3) NP_002974.1:n.*377G>A
XR_001752857.1:n.1637-1251C>T (CCL3-AS1)
XR_001752858.1:n.673-1251C>T (CCL3-AS1)
XR_001752859.1:n.1584-1251C>T (CCL3-AS1)
NM_002983.3:c.*377G>A (CCL3) MANE Select NP_002974.1:n.*377G>A
NR_168494.1:n.1429G>A (CCL3)
NR_168495.1:n.639G>A (CCL3)
NR_168496.1:n.602G>A (CCL3)