Canonical Allele Identifier: CA499710161
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582267C>A (hg19)

Genomic Alleles

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

Transcript Alleles

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