Canonical Allele Identifier: CA499710182
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582274T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255255T>C , CM000679.2:g.34255255T>C GRCh38
NC_000017.10:g.32582274T>C , CM000679.1:g.32582274T>C GRCh37
NC_000017.9:g.29606387T>C NCBI36
NG_012123.1:g.4979T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.38T>C