Canonical Allele Identifier: CA499866744
Gene: CCL3 HGNC NCBI
CCL3-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1846656019
MyVariant Identifiers: chr17:g.34415678T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.36088332T>C , CM000679.2:g.36088332T>C GRCh38
NC_000017.10:g.34415678T>C , CM000679.1:g.34415678T>C GRCh37
NC_000017.9:g.31439791T>C NCBI36
NG_027730.1:g.6829A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000613922.2:c.*340A>G (CCL3) MANE Select ENSP00000477908.1:n.*340A>G
ENST00000613922.1:c.*340A>G (CCL3) ENSP00000477908.1:n.*340A>G
ENST00000613928.1:n.1078A>G (CCL3)
ENST00000614051.1:n.1418A>G (CCL3)
NM_002983.2:c.*340A>G (CCL3) NP_002974.1:n.*340A>G
XR_001752857.1:n.1637-1214T>C (CCL3-AS1)
XR_001752858.1:n.673-1214T>C (CCL3-AS1)
XR_001752859.1:n.1584-1214T>C (CCL3-AS1)
NM_002983.3:c.*340A>G (CCL3) MANE Select NP_002974.1:n.*340A>G
NR_168494.1:n.1392A>G (CCL3)
NR_168495.1:n.602A>G (CCL3)
NR_168496.1:n.565A>G (CCL3)