Canonical Allele Identifier: CA499710232
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582293C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255274C>G , CM000679.2:g.34255274C>G GRCh38
NC_000017.10:g.32582293C>G , CM000679.1:g.32582293C>G GRCh37
NC_000017.9:g.29606406C>G NCBI36
NG_012123.1:g.4998C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.-76C>G ENSP00000462156.1:n.-76C>G
ENST00000624362.1:n.57C>G
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