Canonical Allele Identifier: CA499710160
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs748196460

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255247G>A , CM000679.2:g.34255247G>A GRCh38
NC_000017.10:g.32582266G>A , CM000679.1:g.32582266G>A GRCh37
NC_000017.9:g.29606379G>A NCBI36
NG_012123.1:g.4971G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.30G>A