Canonical Allele Identifier: CA289528667
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1027807658
gnomAD v2: 17-32583338-G-A
gnomAD v3: 17-34256319-G-A
gnomAD v4: 17-34256319-G-A
MyVariant Identifiers: chr17:g.32583338G>A (hg19) chr17:g.34256319G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256319G>A , CM000679.2:g.34256319G>A GRCh38
NC_000017.10:g.32583338G>A , CM000679.1:g.32583338G>A GRCh37
NC_000017.9:g.29607451G>A NCBI36
NG_012123.1:g.6043G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.174G>A ENSP00000462156.1:p.Lys58=
ENST00000624362.2:n.1035G>A
ENST00000225831.4:c.174G>A MANE Select ENSP00000225831.4:p.Lys58=
ENST00000580907.5:c.174G>A ENSP00000462156.1:p.Lys58=
ENST00000582017.1:n.112G>A
NM_002982.3:c.174G>A NP_002973.1:p.Lys58=
NM_002982.4:c.174G>A MANE Select NP_002973.1:p.Lys58=
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