Canonical Allele Identifier: CA499710171
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582270T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255251T>G , CM000679.2:g.34255251T>G GRCh38
NC_000017.10:g.32582270T>G , CM000679.1:g.32582270T>G GRCh37
NC_000017.9:g.29606383T>G NCBI36
NG_012123.1:g.4975T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.34T>G