Canonical Allele Identifier: CA499710190
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582277G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255258G>C , CM000679.2:g.34255258G>C GRCh38
NC_000017.10:g.32582277G>C , CM000679.1:g.32582277G>C GRCh37
NC_000017.9:g.29606390G>C NCBI36
NG_012123.1:g.4982G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.41G>C
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