Canonical Allele Identifier: CA8509984
Gene: CCL3 HGNC NCBI
CCL3-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr17:g.36089191G>A
GRCh37 chr17:g.34416537G>A
gnomAD v2:
17:34416537 G / A
gnomAD v3:
17:36089191 G / A
gnomAD v4:
chr17-36089191-G-A
Joint Max Group AF 0.32071818 (EAS)
Genomes Max Group AF 0.33137664 (EAS)
Exomes Max Group AF 0.31791374 (EAS)
dbSNP:
1130371
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.36089191G>A , CM000679.2:g.36089191G>A GRCh38
NC_000017.10:g.34416537G>A , CM000679.1:g.34416537G>A GRCh37
NC_000017.9:g.31440650G>A NCBI36
NG_027730.1:g.5970C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000613922.2:c.180C>T (CCL3) MANE Select ENSP00000477908.1:p.Pro60=
ENST00000613922.1:c.180C>T (CCL3) ENSP00000477908.1:p.Pro60=
ENST00000613928.1:n.803+141C>T (CCL3)
ENST00000614051.1:n.979C>T (CCL3)
NM_002983.2:c.180C>T (CCL3) NP_002974.1:p.Pro60=
XR_001752857.1:n.1637-355G>A (CCL3-AS1)
XR_001752858.1:n.673-355G>A (CCL3-AS1)
XR_001752859.1:n.1584-355G>A (CCL3-AS1)
NM_002983.3:c.180C>T (CCL3) MANE Select NP_002974.1:p.Pro60=
NR_168494.1:n.953C>T (CCL3)
NR_168495.1:n.163C>T (CCL3)
NR_168496.1:n.126C>T (CCL3)
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