Canonical Allele Identifier: CA983183796
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1907645979

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255227C>T , CM000679.2:g.34255227C>T GRCh38
NC_000017.10:g.32582246C>T , CM000679.1:g.32582246C>T GRCh37
NC_000017.9:g.29606359C>T NCBI36
NG_012123.1:g.4951C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.10C>T