Canonical Allele Identifier: CA290124940
Gene: CCL3 HGNC NCBI
CCL3-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1049191
gnomAD v3: 17-36088473-G-A
gnomAD v4: 17-36088473-G-A
MyVariant Identifiers: chr17:g.34415819G>A (hg19) chr17:g.36088473G>A (hg38)
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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
ENST00000613922.2:c.*199C>T (CCL3) MANE Select ENSP00000477908.1:n.*199C>T
ENST00000613922.1:c.*199C>T (CCL3) ENSP00000477908.1:n.*199C>T
ENST00000613928.1:n.937C>T (CCL3)
ENST00000614051.1:n.1277C>T (CCL3)
NM_002983.2:c.*199C>T (CCL3) NP_002974.1:n.*199C>T
XR_001752857.1:n.1637-1073G>A (CCL3-AS1)
XR_001752858.1:n.673-1073G>A (CCL3-AS1)
XR_001752859.1:n.1584-1073G>A (CCL3-AS1)
NM_002983.3:c.*199C>T (CCL3) MANE Select NP_002974.1:n.*199C>T
NR_168494.1:n.1251C>T (CCL3)
NR_168495.1:n.461C>T (CCL3)
NR_168496.1:n.424C>T (CCL3)
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