Canonical Allele Identifier: CA499710183
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582275A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255256A>C , CM000679.2:g.34255256A>C GRCh38
NC_000017.10:g.32582275A>C , CM000679.1:g.32582275A>C GRCh37
NC_000017.9:g.29606388A>C NCBI36
NG_012123.1:g.4980A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.39A>C