Canonical Allele Identifier: CA499710203
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1238312306

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255263A>G , CM000679.2:g.34255263A>G GRCh38
NC_000017.10:g.32582282A>G , CM000679.1:g.32582282A>G GRCh37
NC_000017.9:g.29606395A>G NCBI36
NG_012123.1:g.4987A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.46A>G