Canonical Allele Identifier: CA728285433
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1159018912
MyVariant Identifiers: chr17:g.32582245C>A (hg19) chr17:g.34255226C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255226C>A , CM000679.2:g.34255226C>A GRCh38
NC_000017.10:g.32582245C>A , CM000679.1:g.32582245C>A GRCh37
NC_000017.9:g.29606358C>A NCBI36
NG_012123.1:g.4950C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.9C>A
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