Canonical Allele Identifier: CA499710240
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582296G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255277G>C , CM000679.2:g.34255277G>C GRCh38
NC_000017.10:g.32582296G>C , CM000679.1:g.32582296G>C GRCh37
NC_000017.9:g.29606409G>C NCBI36
NG_012123.1:g.5001G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.-73G>C ENSP00000462156.1:n.-73G>C
ENST00000624362.1:n.60G>C
NM_002982.3:c.-73G>C NP_002973.1:n.-73G>C