Canonical Allele Identifier: CA499710162
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582267C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255248C>G , CM000679.2:g.34255248C>G GRCh38
NC_000017.10:g.32582267C>G , CM000679.1:g.32582267C>G GRCh37
NC_000017.9:g.29606380C>G NCBI36
NG_012123.1:g.4972C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.31C>G
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