Canonical Allele Identifier: CA2256959472
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1598083028

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255223A>C , CM000679.2:g.34255223A>C GRCh38
NC_000017.10:g.32582242A>C , CM000679.1:g.32582242A>C GRCh37
NC_000017.9:g.29606355A>C NCBI36
NG_012123.1:g.4947A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.6A>C