Canonical Allele Identifier: CA289527959
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs11575012
MyVariant Identifiers: chr17:g.32582250C>G (hg19) chr17:g.34255231C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255231C>G , CM000679.2:g.34255231C>G GRCh38
NC_000017.10:g.32582250C>G , CM000679.1:g.32582250C>G GRCh37
NC_000017.9:g.29606363C>G NCBI36
NG_012123.1:g.4955C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.14C>G
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