Canonical Allele Identifier: CA499710211
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582285G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255266G>A , CM000679.2:g.34255266G>A GRCh38
NC_000017.10:g.32582285G>A , CM000679.1:g.32582285G>A GRCh37
NC_000017.9:g.29606398G>A NCBI36
NG_012123.1:g.4990G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.49G>A
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