Canonical Allele Identifier: CA499710238
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1907648148
MyVariant Identifiers: chr17:g.32582295A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255276A>G , CM000679.2:g.34255276A>G GRCh38
NC_000017.10:g.32582295A>G , CM000679.1:g.32582295A>G GRCh37
NC_000017.9:g.29606408A>G NCBI36
NG_012123.1:g.5000A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.-74A>G ENSP00000462156.1:n.-74A>G
ENST00000624362.1:n.59A>G