Canonical Allele Identifier: CA499710168
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582269T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255250T>C , CM000679.2:g.34255250T>C GRCh38
NC_000017.10:g.32582269T>C , CM000679.1:g.32582269T>C GRCh37
NC_000017.9:g.29606382T>C NCBI36
NG_012123.1:g.4974T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.33T>C