Canonical Allele Identifier: CA290124940
Gene: CCL3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1049191

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.36088473G>A , CM000679.2:g.36088473G>A GRCh38
NC_000017.10:g.34415819G>A , CM000679.1:g.34415819G>A GRCh37
NC_000017.9:g.31439932G>A NCBI36
NG_027730.1:g.6688C>T

Transcript Alleles

HGVS Amino-acid change
NM_002983.2:c.*199C>T VV NP_002974.1:p.=
XR_001752857.1:n.1637-1073G>A
XR_001752858.1:n.673-1073G>A
XR_001752859.1:n.1584-1073G>A
NM_002983.3:c.*199C>T VV MANE Preferred NP_002974.1:p.=
ENST00000613922.1:c.*199C>T ENSP00000477908.1:p.=
ENST00000613928.1:n.937C>T
ENST00000614051.1:n.1277C>T