Canonical Allele Identifier: CA499710231
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582293C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255274C>A , CM000679.2:g.34255274C>A GRCh38
NC_000017.10:g.32582293C>A , CM000679.1:g.32582293C>A GRCh37
NC_000017.9:g.29606406C>A NCBI36
NG_012123.1:g.4998C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.-76C>A ENSP00000462156.1:n.-76C>A
ENST00000624362.1:n.57C>A