Canonical Allele Identifier: CA499710214
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1907647637
MyVariant Identifiers: chr17:g.32582286A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255267A>G , CM000679.2:g.34255267A>G GRCh38
NC_000017.10:g.32582286A>G , CM000679.1:g.32582286A>G GRCh37
NC_000017.9:g.29606399A>G NCBI36
NG_012123.1:g.4991A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.50A>G