Canonical Allele Identifier: CA499710173
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582271C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255252C>A , CM000679.2:g.34255252C>A GRCh38
NC_000017.10:g.32582271C>A , CM000679.1:g.32582271C>A GRCh37
NC_000017.9:g.29606384C>A NCBI36
NG_012123.1:g.4976C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.35C>A